innotest phospho-tau(181p)  (Fujirebio Inc)


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    Fujirebio Inc innotest phospho-tau(181p)
    Innotest Phospho Tau(181p), supplied by Fujirebio Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/innotest phospho-tau(181p)/product/Fujirebio Inc
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    innotest phospho-tau(181p)  (Fujirebio Inc)


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    Fujirebio Inc innotest phospho-tau(181p)
    Innotest Phospho Tau(181p), supplied by Fujirebio Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/innotest phospho-tau(181p)/product/Fujirebio Inc
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    innotest phospho-tau(181p)  (Fujirebio Inc)


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    Fujirebio Inc innotest phospho-tau(181p)
    Innotest Phospho Tau(181p), supplied by Fujirebio Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/innotest phospho-tau(181p)/product/Fujirebio Inc
    Average 96 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    innotest phospho-tau(181p) - by Bioz Stars, 2024-09
    96/100 stars

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    innotest p tau 81574  (Fujirebio Inc)


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    Fujirebio Inc innotest p tau 81574
    Innotest P Tau 81574, supplied by Fujirebio Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Santa Cruz Biotechnology anti per1
    Immunofluorescence photomicrographs of the frontal section of the inferior olivary nucleus (ION) of the primate Sapajus apella showing <t>Per1</t> – IR cells in (A) . Mean of the number of immunoreactive cells to Per1 in 3 brain sections representative of anteroposterior extension of the inferior olivary nucleus (ION) of the primate Sapajus apella ( N = 3 ZT). Photomicrograph of the cytoarchitecture characterization of neuronal populations of the ION represented by fluorescent staining in DAPI (blue) in A1 and B1, overlapping with A. Per-1 antibody showed the specificity of labeling in neuronal populations, allowing the delineation of the ION (A,B) . Per1 in neuronal populations of the ION (C) . Relative number of day and night Per1-IR cells by the surface area of the ION (D) . Intensity of staining - OD (E) . Bar = 100 μm.
    Anti Per1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti per1/product/Santa Cruz Biotechnology
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    1) Product Images from "Melatonin receptors and Per1 expression in the inferior olivary nucleus of the Sapajus apella monkey"

    Article Title: Melatonin receptors and Per1 expression in the inferior olivary nucleus of the Sapajus apella monkey

    Journal: Frontiers in Neuroscience

    doi: 10.3389/fnins.2022.1072772

    Immunofluorescence photomicrographs of the frontal section of the inferior olivary nucleus (ION) of the primate Sapajus apella showing Per1 – IR cells in (A) . Mean of the number of immunoreactive cells to Per1 in 3 brain sections representative of anteroposterior extension of the inferior olivary nucleus (ION) of the primate Sapajus apella ( N = 3 ZT). Photomicrograph of the cytoarchitecture characterization of neuronal populations of the ION represented by fluorescent staining in DAPI (blue) in A1 and B1, overlapping with A. Per-1 antibody showed the specificity of labeling in neuronal populations, allowing the delineation of the ION (A,B) . Per1 in neuronal populations of the ION (C) . Relative number of day and night Per1-IR cells by the surface area of the ION (D) . Intensity of staining - OD (E) . Bar = 100 μm.
    Figure Legend Snippet: Immunofluorescence photomicrographs of the frontal section of the inferior olivary nucleus (ION) of the primate Sapajus apella showing Per1 – IR cells in (A) . Mean of the number of immunoreactive cells to Per1 in 3 brain sections representative of anteroposterior extension of the inferior olivary nucleus (ION) of the primate Sapajus apella ( N = 3 ZT). Photomicrograph of the cytoarchitecture characterization of neuronal populations of the ION represented by fluorescent staining in DAPI (blue) in A1 and B1, overlapping with A. Per-1 antibody showed the specificity of labeling in neuronal populations, allowing the delineation of the ION (A,B) . Per1 in neuronal populations of the ION (C) . Relative number of day and night Per1-IR cells by the surface area of the ION (D) . Intensity of staining - OD (E) . Bar = 100 μm.

    Techniques Used: Immunofluorescence, Staining, Labeling

    innotest phospho-tau(181p)  (Fujirebio Inc)


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    Fujirebio Inc innotest phospho-tau(181p)
    Innotest Phospho Tau(181p), supplied by Fujirebio Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/innotest phospho-tau(181p)/product/Fujirebio Inc
    Average 96 stars, based on 1 article reviews
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    Santa Cruz Biotechnology per1
    Primers of clock and clock controlled genes for qPCR.
    Per1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/per1/product/Santa Cruz Biotechnology
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    per1 - by Bioz Stars, 2024-09
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    1) Product Images from "Oscillation of Clock and Clock Controlled Genes Induced by Serum Shock in Human Breast Epithelial and Breast Cancer Cells: Regulation by Melatonin"

    Article Title: Oscillation of Clock and Clock Controlled Genes Induced by Serum Shock in Human Breast Epithelial and Breast Cancer Cells: Regulation by Melatonin

    Journal: Breast Cancer : Basic and Clinical Research

    doi: 10.4137/BCBCR.S9673

    Primers of clock and clock controlled genes for qPCR.
    Figure Legend Snippet: Primers of clock and clock controlled genes for qPCR.

    Techniques Used:

    Per2 knockdown in MCF-10A cells alters clock gene and CCG expression. MCF-10A Per2 knockdown or control cell lines were generated by infecting MCF-10A cells with Per2 shRNA or control lentiviral particles (Santa Cruz Biotechnology) according to the vendor’s protocol. ( A ) Stably infected cell lines were tested by Western blotting to determine the level of Per2 knockdown, with GAPDH expression used as a measure of protein loading. ( B ) Control and Per2 knockdown MCF-10A cells were plated as described in Materials and Methods and cell proliferation was determined by counting the number number of cells on a heamoctyometer after 4 days. ( C ) qPCR expression of clock and CCGs was determined as control and Per2 knockdown MCF-10A cells were harvested, mRNA extracted, and the clock gene expression for Clock, Bmal1, Per1, Cry1, Cry2, Rev-erbα and clock controlled genes MT 1 , c-Myc, and Sirt1 were analyzed by qPCR. Notes: * P < 0.05 , n = 3.
    Figure Legend Snippet: Per2 knockdown in MCF-10A cells alters clock gene and CCG expression. MCF-10A Per2 knockdown or control cell lines were generated by infecting MCF-10A cells with Per2 shRNA or control lentiviral particles (Santa Cruz Biotechnology) according to the vendor’s protocol. ( A ) Stably infected cell lines were tested by Western blotting to determine the level of Per2 knockdown, with GAPDH expression used as a measure of protein loading. ( B ) Control and Per2 knockdown MCF-10A cells were plated as described in Materials and Methods and cell proliferation was determined by counting the number number of cells on a heamoctyometer after 4 days. ( C ) qPCR expression of clock and CCGs was determined as control and Per2 knockdown MCF-10A cells were harvested, mRNA extracted, and the clock gene expression for Clock, Bmal1, Per1, Cry1, Cry2, Rev-erbα and clock controlled genes MT 1 , c-Myc, and Sirt1 were analyzed by qPCR. Notes: * P < 0.05 , n = 3.

    Techniques Used: Expressing, Generated, shRNA, Stable Transfection, Infection, Western Blot


    Structured Review

    Santa Cruz Biotechnology human clock genes per 1
    Human Clock Genes Per 1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Santa Cruz Biotechnology per1
    Control (cured) OR6 cells and OR6 cells replicating HCV genotype 1b were serum shocked and RNA was extracted every 1 h, 4 h, 10 h, 16 h, 22 h and 28 h after serum shock. mRNA levels of Rev-Erbα, Rorα, ARNTL, ARNTL2, CLOCK, <t>PER1,</t> PER2, PER3, CRY1 and CRY2 genes were assessed by qRT-PCR ( A and B ). Values were normalized against TBP as housekeeping control gene. Results are expressed as means ± SE of three independent experiments. * = p<0.05 in HCV replicating cells versus control cured OR6 cells.
    Per1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Mutual Antagonism between Circadian Protein Period 2 and Hepatitis C Virus Replication in Hepatocytes"

    Article Title: Mutual Antagonism between Circadian Protein Period 2 and Hepatitis C Virus Replication in Hepatocytes

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0060527

    Control (cured) OR6 cells and OR6 cells replicating HCV genotype 1b were serum shocked and RNA was extracted every 1 h, 4 h, 10 h, 16 h, 22 h and 28 h after serum shock. mRNA levels of Rev-Erbα, Rorα, ARNTL, ARNTL2, CLOCK, PER1, PER2, PER3, CRY1 and CRY2 genes were assessed by qRT-PCR ( A and B ). Values were normalized against TBP as housekeeping control gene. Results are expressed as means ± SE of three independent experiments. * = p<0.05 in HCV replicating cells versus control cured OR6 cells.
    Figure Legend Snippet: Control (cured) OR6 cells and OR6 cells replicating HCV genotype 1b were serum shocked and RNA was extracted every 1 h, 4 h, 10 h, 16 h, 22 h and 28 h after serum shock. mRNA levels of Rev-Erbα, Rorα, ARNTL, ARNTL2, CLOCK, PER1, PER2, PER3, CRY1 and CRY2 genes were assessed by qRT-PCR ( A and B ). Values were normalized against TBP as housekeeping control gene. Results are expressed as means ± SE of three independent experiments. * = p<0.05 in HCV replicating cells versus control cured OR6 cells.

    Techniques Used: Quantitative RT-PCR

    Huh-7 cells were transiently transfected with HCV core proteins 1b and 3a as previously described , or with GFP. 48 hours after transfection mRNA levels of Rev-Erbα, Rorα, ARNTL, ARNTL2, CLOCK, PER1, PER2, PER3, CRY1 and CRY2 genes were assessed by qRT-PCR. Values were normalized against TBP as housekeeping control gene. Light gray: GFP transfected cells; dark gray: HCV core protein genotype 3a transfected cells; black: HCV core protein genotype 1b transfected cells. Results are expressed as means ± SE of three independent experiments. * = p<0.05 in HCV core proteins transfected versus GFP transfected control cells.
    Figure Legend Snippet: Huh-7 cells were transiently transfected with HCV core proteins 1b and 3a as previously described , or with GFP. 48 hours after transfection mRNA levels of Rev-Erbα, Rorα, ARNTL, ARNTL2, CLOCK, PER1, PER2, PER3, CRY1 and CRY2 genes were assessed by qRT-PCR. Values were normalized against TBP as housekeeping control gene. Light gray: GFP transfected cells; dark gray: HCV core protein genotype 3a transfected cells; black: HCV core protein genotype 1b transfected cells. Results are expressed as means ± SE of three independent experiments. * = p<0.05 in HCV core proteins transfected versus GFP transfected control cells.

    Techniques Used: Transfection, Quantitative RT-PCR

    ( A ) 48 hours after transfection cells were lysed and equal amounts of proteins were loaded on a 10% polyacrylamide gel, separated by electrophoresis and immunoblotted with specific Rev-Erbα, Rorα, CLOCK, ARNTL, ARNTL2, PER1, PER2, CRY1 and CRY2 primary antibodies. β-actin expression served as loading control. ( B ) Densitometric quantification of CRY2, PER2 and CLOCK proteins normalized to β-actin expression of three different experiments.
    Figure Legend Snippet: ( A ) 48 hours after transfection cells were lysed and equal amounts of proteins were loaded on a 10% polyacrylamide gel, separated by electrophoresis and immunoblotted with specific Rev-Erbα, Rorα, CLOCK, ARNTL, ARNTL2, PER1, PER2, CRY1 and CRY2 primary antibodies. β-actin expression served as loading control. ( B ) Densitometric quantification of CRY2, PER2 and CLOCK proteins normalized to β-actin expression of three different experiments.

    Techniques Used: Transfection, Electrophoresis, Expressing


    Structured Review

    Santa Cruz Biotechnology per1 antibody
    Photomicrographs showing expression of FOS (A, B) and <t>PER1</t> (C,D) in nursed subjects at 02∶00 (A,C) or 10∶00 (B,D) h. Note that FOS is high at time of nursing (ZT0) and 1.5 h later (ZT1.5), and PER1 is high 8 h after nursing (ZT08). Dotted lines delimit the layers. G, Granular cell layer; M, Mitral cell layer; PG, periglomerular cell layer. Rectangles represent the counted area. Scale bar, 100 μm.
    Per1 Antibody, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/per1 antibody/product/Santa Cruz Biotechnology
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    1) Product Images from "A Circadian Clock in the Olfactory Bulb Anticipates Feeding during Food Anticipatory Activity"

    Article Title: A Circadian Clock in the Olfactory Bulb Anticipates Feeding during Food Anticipatory Activity

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0047779

    Photomicrographs showing expression of FOS (A, B) and PER1 (C,D) in nursed subjects at 02∶00 (A,C) or 10∶00 (B,D) h. Note that FOS is high at time of nursing (ZT0) and 1.5 h later (ZT1.5), and PER1 is high 8 h after nursing (ZT08). Dotted lines delimit the layers. G, Granular cell layer; M, Mitral cell layer; PG, periglomerular cell layer. Rectangles represent the counted area. Scale bar, 100 μm.
    Figure Legend Snippet: Photomicrographs showing expression of FOS (A, B) and PER1 (C,D) in nursed subjects at 02∶00 (A,C) or 10∶00 (B,D) h. Note that FOS is high at time of nursing (ZT0) and 1.5 h later (ZT1.5), and PER1 is high 8 h after nursing (ZT08). Dotted lines delimit the layers. G, Granular cell layer; M, Mitral cell layer; PG, periglomerular cell layer. Rectangles represent the counted area. Scale bar, 100 μm.

    Techniques Used: Expressing

    Graphs show PER1 expression in the periglomerular, mitral and granular layers in pups nursed and fasted during the night (A, C, E) or during the day (B, D, F). The acrophase of PER1 expression was 4–8 h after nursing time. Values are mean ± SEM. * Significant difference between highest and lowest values in each group. **, P<0.01 (see text for details).
    Figure Legend Snippet: Graphs show PER1 expression in the periglomerular, mitral and granular layers in pups nursed and fasted during the night (A, C, E) or during the day (B, D, F). The acrophase of PER1 expression was 4–8 h after nursing time. Values are mean ± SEM. * Significant difference between highest and lowest values in each group. **, P<0.01 (see text for details).

    Techniques Used: Expressing

    Photomicrographs showing expression of FOS (A) and PER1 (B) at times of high (ZT1.5; ZT08) and low (ZT20) proteins expression. Dotted lines delimit the mitral cell layer (M). Scale bar, 100 μm.
    Figure Legend Snippet: Photomicrographs showing expression of FOS (A) and PER1 (B) at times of high (ZT1.5; ZT08) and low (ZT20) proteins expression. Dotted lines delimit the mitral cell layer (M). Scale bar, 100 μm.

    Techniques Used: Expressing

    Graphs shows FOS (A, B) and PER1 (C, D) in the mitral cell layer in pups nursed and fasted during the night (A, C) or during the day (B, D). Note that FOS expression is high at the time of nursing and increases further 1.5 h later. PER1 expression has a rhythm only in RF10∶00 group with an increase 8 h after nursing. Values are mean ± SEM. * Significant difference between highest and lowest values in each group. + + Significant difference of ZT0 and ZT04 time points against the lowest values. **, ++, P<0.01 (see text for details).
    Figure Legend Snippet: Graphs shows FOS (A, B) and PER1 (C, D) in the mitral cell layer in pups nursed and fasted during the night (A, C) or during the day (B, D). Note that FOS expression is high at the time of nursing and increases further 1.5 h later. PER1 expression has a rhythm only in RF10∶00 group with an increase 8 h after nursing. Values are mean ± SEM. * Significant difference between highest and lowest values in each group. + + Significant difference of ZT0 and ZT04 time points against the lowest values. **, ++, P<0.01 (see text for details).

    Techniques Used: Expressing


    Structured Review

    Santa Cruz Biotechnology antibodies against per1
    Daily rhythm characteristics of plasma corticosterone and <t> PER1 </t> from rats under free access meal and restricted schedule determined by COSINOR test
    Antibodies Against Per1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/antibodies against per1/product/Santa Cruz Biotechnology
    Average 93 stars, based on 1 article reviews
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    Images

    1) Product Images from "Diurnal and nutritional adjustments of intracellular Ca 2+ release channels and Ca 2+ ATPases associated with restricted feeding schedules in the rat liver"

    Article Title: Diurnal and nutritional adjustments of intracellular Ca 2+ release channels and Ca 2+ ATPases associated with restricted feeding schedules in the rat liver

    Journal: Journal of Circadian Rhythms

    doi: 10.1186/1740-3391-11-8

    Daily rhythm characteristics of plasma corticosterone and  PER1  from rats under free access meal and restricted schedule determined by COSINOR test
    Figure Legend Snippet: Daily rhythm characteristics of plasma corticosterone and PER1 from rats under free access meal and restricted schedule determined by COSINOR test

    Techniques Used:

    Serum corticosterone and PER1 protein levels are entrained by food access. Diurnal corticosterone levels in rats fed ad libitum (AL) and under RF are shown in panel A. Quantitative analysis of clock protein PER1 using 50 μg of cytosolic fraction from at least 4 individuals is represented in panel B. Each value was normalized using the housekeeping protein actin as reference, and a representative western blot for each condition is shown. Black circles correspond to AL and white circles to RF group. The light gray rectangle above the x-axis represents mealtime for the food restricted group (ZT4-ZT6); * ( p < 0.05) means significant difference among AL group time points and + ( p < 0.05) significant difference among RF group time points (1-way ANOVA). # ( p < 0.05) significant difference between AL vs RF (2-way ANOVA).
    Figure Legend Snippet: Serum corticosterone and PER1 protein levels are entrained by food access. Diurnal corticosterone levels in rats fed ad libitum (AL) and under RF are shown in panel A. Quantitative analysis of clock protein PER1 using 50 μg of cytosolic fraction from at least 4 individuals is represented in panel B. Each value was normalized using the housekeeping protein actin as reference, and a representative western blot for each condition is shown. Black circles correspond to AL and white circles to RF group. The light gray rectangle above the x-axis represents mealtime for the food restricted group (ZT4-ZT6); * ( p < 0.05) means significant difference among AL group time points and + ( p < 0.05) significant difference among RF group time points (1-way ANOVA). # ( p < 0.05) significant difference between AL vs RF (2-way ANOVA).

    Techniques Used: Western Blot

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    Fujirebio Inc innotest phospho-tau(181p)
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    Santa Cruz Biotechnology anti per1
    Immunofluorescence photomicrographs of the frontal section of the inferior olivary nucleus (ION) of the primate Sapajus apella showing <t>Per1</t> – IR cells in (A) . Mean of the number of immunoreactive cells to Per1 in 3 brain sections representative of anteroposterior extension of the inferior olivary nucleus (ION) of the primate Sapajus apella ( N = 3 ZT). Photomicrograph of the cytoarchitecture characterization of neuronal populations of the ION represented by fluorescent staining in DAPI (blue) in A1 and B1, overlapping with A. Per-1 antibody showed the specificity of labeling in neuronal populations, allowing the delineation of the ION (A,B) . Per1 in neuronal populations of the ION (C) . Relative number of day and night Per1-IR cells by the surface area of the ION (D) . Intensity of staining - OD (E) . Bar = 100 μm.
    Anti Per1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Santa Cruz Biotechnology per1
    Primers of clock and clock controlled genes for qPCR.
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    Santa Cruz Biotechnology human clock genes per 1
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    Human Clock Genes Per 1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Santa Cruz Biotechnology per1 antibody
    Photomicrographs showing expression of FOS (A, B) and <t>PER1</t> (C,D) in nursed subjects at 02∶00 (A,C) or 10∶00 (B,D) h. Note that FOS is high at time of nursing (ZT0) and 1.5 h later (ZT1.5), and PER1 is high 8 h after nursing (ZT08). Dotted lines delimit the layers. G, Granular cell layer; M, Mitral cell layer; PG, periglomerular cell layer. Rectangles represent the counted area. Scale bar, 100 μm.
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    Santa Cruz Biotechnology antibodies against per1
    Daily rhythm characteristics of plasma corticosterone and <t> PER1 </t> from rats under free access meal and restricted schedule determined by COSINOR test
    Antibodies Against Per1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Immunofluorescence photomicrographs of the frontal section of the inferior olivary nucleus (ION) of the primate Sapajus apella showing Per1 – IR cells in (A) . Mean of the number of immunoreactive cells to Per1 in 3 brain sections representative of anteroposterior extension of the inferior olivary nucleus (ION) of the primate Sapajus apella ( N = 3 ZT). Photomicrograph of the cytoarchitecture characterization of neuronal populations of the ION represented by fluorescent staining in DAPI (blue) in A1 and B1, overlapping with A. Per-1 antibody showed the specificity of labeling in neuronal populations, allowing the delineation of the ION (A,B) . Per1 in neuronal populations of the ION (C) . Relative number of day and night Per1-IR cells by the surface area of the ION (D) . Intensity of staining - OD (E) . Bar = 100 μm.

    Journal: Frontiers in Neuroscience

    Article Title: Melatonin receptors and Per1 expression in the inferior olivary nucleus of the Sapajus apella monkey

    doi: 10.3389/fnins.2022.1072772

    Figure Lengend Snippet: Immunofluorescence photomicrographs of the frontal section of the inferior olivary nucleus (ION) of the primate Sapajus apella showing Per1 – IR cells in (A) . Mean of the number of immunoreactive cells to Per1 in 3 brain sections representative of anteroposterior extension of the inferior olivary nucleus (ION) of the primate Sapajus apella ( N = 3 ZT). Photomicrograph of the cytoarchitecture characterization of neuronal populations of the ION represented by fluorescent staining in DAPI (blue) in A1 and B1, overlapping with A. Per-1 antibody showed the specificity of labeling in neuronal populations, allowing the delineation of the ION (A,B) . Per1 in neuronal populations of the ION (C) . Relative number of day and night Per1-IR cells by the surface area of the ION (D) . Intensity of staining - OD (E) . Bar = 100 μm.

    Article Snippet: The sections were washed using a solution TBS-TX buffer (0.05 M), incubated for 48 h at 4°C in a solution containing 0.05 M TBS-TX buffer, 2% normal serum (Vector Laboratories, USA), and the appropriate primary antibody: anti-MT1 (1: 200, Santa Cruz), anti-MT2 (1: 200, Santa Cruz), anti-Per1 (1:500, Santa Cruz, USA) separately.

    Techniques: Immunofluorescence, Staining, Labeling

    Primers of clock and clock controlled genes for qPCR.

    Journal: Breast Cancer : Basic and Clinical Research

    Article Title: Oscillation of Clock and Clock Controlled Genes Induced by Serum Shock in Human Breast Epithelial and Breast Cancer Cells: Regulation by Melatonin

    doi: 10.4137/BCBCR.S9673

    Figure Lengend Snippet: Primers of clock and clock controlled genes for qPCR.

    Article Snippet: Monoclonal antibodies against human CLOCK, BMAL1, PER1, PER2, CRY1 and CRY2 proteins were purchased from Santa Cruz Biotechnology (Santa Cruz, CA), and a mouse antibody against GAPDH was purchased from Sigma Chemical Co. (St. Louis, MO).

    Techniques:

    Per2 knockdown in MCF-10A cells alters clock gene and CCG expression. MCF-10A Per2 knockdown or control cell lines were generated by infecting MCF-10A cells with Per2 shRNA or control lentiviral particles (Santa Cruz Biotechnology) according to the vendor’s protocol. ( A ) Stably infected cell lines were tested by Western blotting to determine the level of Per2 knockdown, with GAPDH expression used as a measure of protein loading. ( B ) Control and Per2 knockdown MCF-10A cells were plated as described in Materials and Methods and cell proliferation was determined by counting the number number of cells on a heamoctyometer after 4 days. ( C ) qPCR expression of clock and CCGs was determined as control and Per2 knockdown MCF-10A cells were harvested, mRNA extracted, and the clock gene expression for Clock, Bmal1, Per1, Cry1, Cry2, Rev-erbα and clock controlled genes MT 1 , c-Myc, and Sirt1 were analyzed by qPCR. Notes: * P < 0.05 , n = 3.

    Journal: Breast Cancer : Basic and Clinical Research

    Article Title: Oscillation of Clock and Clock Controlled Genes Induced by Serum Shock in Human Breast Epithelial and Breast Cancer Cells: Regulation by Melatonin

    doi: 10.4137/BCBCR.S9673

    Figure Lengend Snippet: Per2 knockdown in MCF-10A cells alters clock gene and CCG expression. MCF-10A Per2 knockdown or control cell lines were generated by infecting MCF-10A cells with Per2 shRNA or control lentiviral particles (Santa Cruz Biotechnology) according to the vendor’s protocol. ( A ) Stably infected cell lines were tested by Western blotting to determine the level of Per2 knockdown, with GAPDH expression used as a measure of protein loading. ( B ) Control and Per2 knockdown MCF-10A cells were plated as described in Materials and Methods and cell proliferation was determined by counting the number number of cells on a heamoctyometer after 4 days. ( C ) qPCR expression of clock and CCGs was determined as control and Per2 knockdown MCF-10A cells were harvested, mRNA extracted, and the clock gene expression for Clock, Bmal1, Per1, Cry1, Cry2, Rev-erbα and clock controlled genes MT 1 , c-Myc, and Sirt1 were analyzed by qPCR. Notes: * P < 0.05 , n = 3.

    Article Snippet: Monoclonal antibodies against human CLOCK, BMAL1, PER1, PER2, CRY1 and CRY2 proteins were purchased from Santa Cruz Biotechnology (Santa Cruz, CA), and a mouse antibody against GAPDH was purchased from Sigma Chemical Co. (St. Louis, MO).

    Techniques: Expressing, Generated, shRNA, Stable Transfection, Infection, Western Blot

    Photomicrographs showing expression of FOS (A, B) and PER1 (C,D) in nursed subjects at 02∶00 (A,C) or 10∶00 (B,D) h. Note that FOS is high at time of nursing (ZT0) and 1.5 h later (ZT1.5), and PER1 is high 8 h after nursing (ZT08). Dotted lines delimit the layers. G, Granular cell layer; M, Mitral cell layer; PG, periglomerular cell layer. Rectangles represent the counted area. Scale bar, 100 μm.

    Journal: PLoS ONE

    Article Title: A Circadian Clock in the Olfactory Bulb Anticipates Feeding during Food Anticipatory Activity

    doi: 10.1371/journal.pone.0047779

    Figure Lengend Snippet: Photomicrographs showing expression of FOS (A, B) and PER1 (C,D) in nursed subjects at 02∶00 (A,C) or 10∶00 (B,D) h. Note that FOS is high at time of nursing (ZT0) and 1.5 h later (ZT1.5), and PER1 is high 8 h after nursing (ZT08). Dotted lines delimit the layers. G, Granular cell layer; M, Mitral cell layer; PG, periglomerular cell layer. Rectangles represent the counted area. Scale bar, 100 μm.

    Article Snippet: Free floating sections were incubated in PER1 antibody raised in goat (sc-7724, Santa Cruz Biotechnology, Santa Cruz, CA, USA) or in c-Fos antibody raised in goat (sc-52G, Santa Cruz Biotechnology, Santa Cruz, CA, USA) both diluted at 1∶2000, in 3% normal horse serum and 0.3% Triton X-100 (Sigma, St. Louis MO, USA), for 48 h at 4°C.

    Techniques: Expressing

    Graphs show PER1 expression in the periglomerular, mitral and granular layers in pups nursed and fasted during the night (A, C, E) or during the day (B, D, F). The acrophase of PER1 expression was 4–8 h after nursing time. Values are mean ± SEM. * Significant difference between highest and lowest values in each group. **, P<0.01 (see text for details).

    Journal: PLoS ONE

    Article Title: A Circadian Clock in the Olfactory Bulb Anticipates Feeding during Food Anticipatory Activity

    doi: 10.1371/journal.pone.0047779

    Figure Lengend Snippet: Graphs show PER1 expression in the periglomerular, mitral and granular layers in pups nursed and fasted during the night (A, C, E) or during the day (B, D, F). The acrophase of PER1 expression was 4–8 h after nursing time. Values are mean ± SEM. * Significant difference between highest and lowest values in each group. **, P<0.01 (see text for details).

    Article Snippet: Free floating sections were incubated in PER1 antibody raised in goat (sc-7724, Santa Cruz Biotechnology, Santa Cruz, CA, USA) or in c-Fos antibody raised in goat (sc-52G, Santa Cruz Biotechnology, Santa Cruz, CA, USA) both diluted at 1∶2000, in 3% normal horse serum and 0.3% Triton X-100 (Sigma, St. Louis MO, USA), for 48 h at 4°C.

    Techniques: Expressing

    Photomicrographs showing expression of FOS (A) and PER1 (B) at times of high (ZT1.5; ZT08) and low (ZT20) proteins expression. Dotted lines delimit the mitral cell layer (M). Scale bar, 100 μm.

    Journal: PLoS ONE

    Article Title: A Circadian Clock in the Olfactory Bulb Anticipates Feeding during Food Anticipatory Activity

    doi: 10.1371/journal.pone.0047779

    Figure Lengend Snippet: Photomicrographs showing expression of FOS (A) and PER1 (B) at times of high (ZT1.5; ZT08) and low (ZT20) proteins expression. Dotted lines delimit the mitral cell layer (M). Scale bar, 100 μm.

    Article Snippet: Free floating sections were incubated in PER1 antibody raised in goat (sc-7724, Santa Cruz Biotechnology, Santa Cruz, CA, USA) or in c-Fos antibody raised in goat (sc-52G, Santa Cruz Biotechnology, Santa Cruz, CA, USA) both diluted at 1∶2000, in 3% normal horse serum and 0.3% Triton X-100 (Sigma, St. Louis MO, USA), for 48 h at 4°C.

    Techniques: Expressing

    Graphs shows FOS (A, B) and PER1 (C, D) in the mitral cell layer in pups nursed and fasted during the night (A, C) or during the day (B, D). Note that FOS expression is high at the time of nursing and increases further 1.5 h later. PER1 expression has a rhythm only in RF10∶00 group with an increase 8 h after nursing. Values are mean ± SEM. * Significant difference between highest and lowest values in each group. + + Significant difference of ZT0 and ZT04 time points against the lowest values. **, ++, P<0.01 (see text for details).

    Journal: PLoS ONE

    Article Title: A Circadian Clock in the Olfactory Bulb Anticipates Feeding during Food Anticipatory Activity

    doi: 10.1371/journal.pone.0047779

    Figure Lengend Snippet: Graphs shows FOS (A, B) and PER1 (C, D) in the mitral cell layer in pups nursed and fasted during the night (A, C) or during the day (B, D). Note that FOS expression is high at the time of nursing and increases further 1.5 h later. PER1 expression has a rhythm only in RF10∶00 group with an increase 8 h after nursing. Values are mean ± SEM. * Significant difference between highest and lowest values in each group. + + Significant difference of ZT0 and ZT04 time points against the lowest values. **, ++, P<0.01 (see text for details).

    Article Snippet: Free floating sections were incubated in PER1 antibody raised in goat (sc-7724, Santa Cruz Biotechnology, Santa Cruz, CA, USA) or in c-Fos antibody raised in goat (sc-52G, Santa Cruz Biotechnology, Santa Cruz, CA, USA) both diluted at 1∶2000, in 3% normal horse serum and 0.3% Triton X-100 (Sigma, St. Louis MO, USA), for 48 h at 4°C.

    Techniques: Expressing

    Daily rhythm characteristics of plasma corticosterone and  PER1  from rats under free access meal and restricted schedule determined by COSINOR test

    Journal: Journal of Circadian Rhythms

    Article Title: Diurnal and nutritional adjustments of intracellular Ca 2+ release channels and Ca 2+ ATPases associated with restricted feeding schedules in the rat liver

    doi: 10.1186/1740-3391-11-8

    Figure Lengend Snippet: Daily rhythm characteristics of plasma corticosterone and PER1 from rats under free access meal and restricted schedule determined by COSINOR test

    Article Snippet: Antibodies against PER1 (sc-7724), IP 3 R1(sc-6093) and IP 3 R2 (sc-7278), SERCA2 (sc-8094), PMCA1 (sc-16488) and PMCA4 (sc-22080), and Actin as well as alkaline phosphatase (AP)-conjugated rabbit anti-goat and goat anti-mouse secondary antibodies were obtained from Santa Cruz Biotechnology (Santa Cruz, CA, USA), and the Ryanodine Receptor (ab9078) was from Millipore (MA, USA).

    Techniques:

    Serum corticosterone and PER1 protein levels are entrained by food access. Diurnal corticosterone levels in rats fed ad libitum (AL) and under RF are shown in panel A. Quantitative analysis of clock protein PER1 using 50 μg of cytosolic fraction from at least 4 individuals is represented in panel B. Each value was normalized using the housekeeping protein actin as reference, and a representative western blot for each condition is shown. Black circles correspond to AL and white circles to RF group. The light gray rectangle above the x-axis represents mealtime for the food restricted group (ZT4-ZT6); * ( p < 0.05) means significant difference among AL group time points and + ( p < 0.05) significant difference among RF group time points (1-way ANOVA). # ( p < 0.05) significant difference between AL vs RF (2-way ANOVA).

    Journal: Journal of Circadian Rhythms

    Article Title: Diurnal and nutritional adjustments of intracellular Ca 2+ release channels and Ca 2+ ATPases associated with restricted feeding schedules in the rat liver

    doi: 10.1186/1740-3391-11-8

    Figure Lengend Snippet: Serum corticosterone and PER1 protein levels are entrained by food access. Diurnal corticosterone levels in rats fed ad libitum (AL) and under RF are shown in panel A. Quantitative analysis of clock protein PER1 using 50 μg of cytosolic fraction from at least 4 individuals is represented in panel B. Each value was normalized using the housekeeping protein actin as reference, and a representative western blot for each condition is shown. Black circles correspond to AL and white circles to RF group. The light gray rectangle above the x-axis represents mealtime for the food restricted group (ZT4-ZT6); * ( p < 0.05) means significant difference among AL group time points and + ( p < 0.05) significant difference among RF group time points (1-way ANOVA). # ( p < 0.05) significant difference between AL vs RF (2-way ANOVA).

    Article Snippet: Antibodies against PER1 (sc-7724), IP 3 R1(sc-6093) and IP 3 R2 (sc-7278), SERCA2 (sc-8094), PMCA1 (sc-16488) and PMCA4 (sc-22080), and Actin as well as alkaline phosphatase (AP)-conjugated rabbit anti-goat and goat anti-mouse secondary antibodies were obtained from Santa Cruz Biotechnology (Santa Cruz, CA, USA), and the Ryanodine Receptor (ab9078) was from Millipore (MA, USA).

    Techniques: Western Blot