t akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc t akt
    T Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    t akt cell signalling  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc t akt cell signalling
    T Akt Cell Signalling, supplied by Cell Signaling Technology 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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    t akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc t akt
    T Akt, supplied by Cell Signaling Technology 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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    t akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc t akt
    a and b WT and Slc37a2 KO BMM-derived osteoclasts were TRAP stained ( a ), and TRAP activity measured (405 nm) ( b ) ( n = 3). Bar, 50 µm. c Representative images of WT and Slc37a2 KO osteoclasts immunostained for F-actin, αvβ3 (IntegriSense 645 ) and nuclei. Bar 50 µm. d Expression of osteoclast and SL markers during RANKL-induced differentiation of WT and Slc37a2 KO BMMs by immunoblotting using indicated antibodies ( n = 3). e RANKL-signaling in WT and Slc37a2 KO BMMs. Immunoblotting of the levels and phosphorylation states <t>of</t> <t>ERK1/2,</t> <t>AKT,</t> and IκBα in response to RANKL ( n = 3). f Representative Von Kossa staining of WT and Slc37a2 KO osteoclasts on mineralized substrates ( n = 3). g–m Representative images of in vitro bone resorption assays of WT and Slc37a2 KO osteoclasts using reflective microscopy, SEM, and confocal microscopy with quantification of the percentage of eroded surface ( h , n = 11 bone discs from 3 experiments; P = 0.0004), pit area ( i , n = 11 bone discs from 3 experiments; P = 0.0029), trench surface per bone slice ( j , n = 11 bone discs from 3 experiments; P = 0.0006), trench surface/eroded surface ( k , n = 11 bone discs from 3 experiments; P < 0.0001), collagen1a staining ( l , n = 12 bone discs from 3 experiments; P < 0.0001) and a number of F-actin rings per bone slice ( m , n = 12 bone discs fro m 3 experiments; P = 0.9293). Black and white arrows indicate bone resorption pits in toluidine blue and collagen 1 stained bone slices, respectively. Bars, 50 µm. n and o Rescue of Slc37a2 KO osteoclasts activity by lentiviral transduction of emGFP- Slc37a2. Depicted are representative images of toluidine blue stained resorptive pits of WT, Slc37a2 KO , and emGFP- Slc37a2 transduced Slc37a2 KO osteoclasts with quantification of the percentage resorbed surface per field quantified ( n = 54 fields from 3 experiments, WT vs. Slc37a2 KO P < 0.0001; WT vs. emGF P- Slc37a2 KO P = 0.0011; Slc37a2 KO vs. emGFP- Slc37a2 KO P = 0.0250). All data are presented as means ± SD. * P < 0.05, ** P < 0.01, *** P < 0.001 by two-tailed unpaired Student’s t- test ( h – m ) or nested one-way ANOVA ( o ). Bar, 50 µm. Source data are available in the Source Data file.
    T Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/t akt/product/Cell Signaling Technology Inc
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    Images

    1) Product Images from "Sugar transporter Slc37a2 regulates bone metabolism in mice via a tubular lysosomal network in osteoclasts"

    Article Title: Sugar transporter Slc37a2 regulates bone metabolism in mice via a tubular lysosomal network in osteoclasts

    Journal: Nature Communications

    doi: 10.1038/s41467-023-36484-2

    a and b WT and Slc37a2 KO BMM-derived osteoclasts were TRAP stained ( a ), and TRAP activity measured (405 nm) ( b ) ( n = 3). Bar, 50 µm. c Representative images of WT and Slc37a2 KO osteoclasts immunostained for F-actin, αvβ3 (IntegriSense 645 ) and nuclei. Bar 50 µm. d Expression of osteoclast and SL markers during RANKL-induced differentiation of WT and Slc37a2 KO BMMs by immunoblotting using indicated antibodies ( n = 3). e RANKL-signaling in WT and Slc37a2 KO BMMs. Immunoblotting of the levels and phosphorylation states of ERK1/2, AKT, and IκBα in response to RANKL ( n = 3). f Representative Von Kossa staining of WT and Slc37a2 KO osteoclasts on mineralized substrates ( n = 3). g–m Representative images of in vitro bone resorption assays of WT and Slc37a2 KO osteoclasts using reflective microscopy, SEM, and confocal microscopy with quantification of the percentage of eroded surface ( h , n = 11 bone discs from 3 experiments; P = 0.0004), pit area ( i , n = 11 bone discs from 3 experiments; P = 0.0029), trench surface per bone slice ( j , n = 11 bone discs from 3 experiments; P = 0.0006), trench surface/eroded surface ( k , n = 11 bone discs from 3 experiments; P < 0.0001), collagen1a staining ( l , n = 12 bone discs from 3 experiments; P < 0.0001) and a number of F-actin rings per bone slice ( m , n = 12 bone discs fro m 3 experiments; P = 0.9293). Black and white arrows indicate bone resorption pits in toluidine blue and collagen 1 stained bone slices, respectively. Bars, 50 µm. n and o Rescue of Slc37a2 KO osteoclasts activity by lentiviral transduction of emGFP- Slc37a2. Depicted are representative images of toluidine blue stained resorptive pits of WT, Slc37a2 KO , and emGFP- Slc37a2 transduced Slc37a2 KO osteoclasts with quantification of the percentage resorbed surface per field quantified ( n = 54 fields from 3 experiments, WT vs. Slc37a2 KO P < 0.0001; WT vs. emGF P- Slc37a2 KO P = 0.0011; Slc37a2 KO vs. emGFP- Slc37a2 KO P = 0.0250). All data are presented as means ± SD. * P < 0.05, ** P < 0.01, *** P < 0.001 by two-tailed unpaired Student’s t- test ( h – m ) or nested one-way ANOVA ( o ). Bar, 50 µm. Source data are available in the Source Data file.
    Figure Legend Snippet: a and b WT and Slc37a2 KO BMM-derived osteoclasts were TRAP stained ( a ), and TRAP activity measured (405 nm) ( b ) ( n = 3). Bar, 50 µm. c Representative images of WT and Slc37a2 KO osteoclasts immunostained for F-actin, αvβ3 (IntegriSense 645 ) and nuclei. Bar 50 µm. d Expression of osteoclast and SL markers during RANKL-induced differentiation of WT and Slc37a2 KO BMMs by immunoblotting using indicated antibodies ( n = 3). e RANKL-signaling in WT and Slc37a2 KO BMMs. Immunoblotting of the levels and phosphorylation states of ERK1/2, AKT, and IκBα in response to RANKL ( n = 3). f Representative Von Kossa staining of WT and Slc37a2 KO osteoclasts on mineralized substrates ( n = 3). g–m Representative images of in vitro bone resorption assays of WT and Slc37a2 KO osteoclasts using reflective microscopy, SEM, and confocal microscopy with quantification of the percentage of eroded surface ( h , n = 11 bone discs from 3 experiments; P = 0.0004), pit area ( i , n = 11 bone discs from 3 experiments; P = 0.0029), trench surface per bone slice ( j , n = 11 bone discs from 3 experiments; P = 0.0006), trench surface/eroded surface ( k , n = 11 bone discs from 3 experiments; P < 0.0001), collagen1a staining ( l , n = 12 bone discs from 3 experiments; P < 0.0001) and a number of F-actin rings per bone slice ( m , n = 12 bone discs fro m 3 experiments; P = 0.9293). Black and white arrows indicate bone resorption pits in toluidine blue and collagen 1 stained bone slices, respectively. Bars, 50 µm. n and o Rescue of Slc37a2 KO osteoclasts activity by lentiviral transduction of emGFP- Slc37a2. Depicted are representative images of toluidine blue stained resorptive pits of WT, Slc37a2 KO , and emGFP- Slc37a2 transduced Slc37a2 KO osteoclasts with quantification of the percentage resorbed surface per field quantified ( n = 54 fields from 3 experiments, WT vs. Slc37a2 KO P < 0.0001; WT vs. emGF P- Slc37a2 KO P = 0.0011; Slc37a2 KO vs. emGFP- Slc37a2 KO P = 0.0250). All data are presented as means ± SD. * P < 0.05, ** P < 0.01, *** P < 0.001 by two-tailed unpaired Student’s t- test ( h – m ) or nested one-way ANOVA ( o ). Bar, 50 µm. Source data are available in the Source Data file.

    Techniques Used: Derivative Assay, Staining, Activity Assay, Expressing, Western Blot, In Vitro, Microscopy, Confocal Microscopy, Transduction, Two Tailed Test

    rabbit monoclonal anti t akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit monoclonal anti t akt
    KEY RESOURCES TABLE
    Rabbit Monoclonal Anti T Akt, supplied by Cell Signaling Technology 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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    1) Product Images from "HIF-1α accumulation in response to transient hypoglycemia may worsen diabetic eye disease"

    Article Title: HIF-1α accumulation in response to transient hypoglycemia may worsen diabetic eye disease

    Journal: Cell reports

    doi: 10.1016/j.celrep.2022.111976

    KEY RESOURCES TABLE
    Figure Legend Snippet: KEY RESOURCES TABLE

    Techniques Used: Recombinant, Tube Formation Assay, In Vivo, Angiogenesis Assay, Enzyme-linked Immunosorbent Assay, Nad NADH Assay, Lactate Assay, Plasmid Preparation, Software

    t akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc t akt
    T Akt, supplied by Cell Signaling Technology 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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    anti phospho akt substrate rxxs t  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti phospho akt substrate rxxs t
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    t akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc t akt
    T Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti t akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti t akt
    Anti T Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    s t protein kinase akt  (Cell Signaling Technology Inc)


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    t akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc t akt
    T Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    KEY RESOURCES TABLE

    Journal: Cell reports

    Article Title: HIF-1α accumulation in response to transient hypoglycemia may worsen diabetic eye disease

    doi: 10.1016/j.celrep.2022.111976

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Rabbit monoclonal anti-t-AKT , Cell Signaling , Cat# 4691; RRID:AB_915783.

    Techniques: Recombinant, Tube Formation Assay, In Vivo, Angiogenesis Assay, Enzyme-linked Immunosorbent Assay, Nad NADH Assay, Lactate Assay, Plasmid Preparation, Software