creatine Search Results


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Novus Biologicals anti-ckb
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R&D Systems creatine kinase b
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Novus Biologicals serum ck mb concentration
Serum Ck Mb Concentration, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cusabio rat creatine kinase mb ck mb elisa kit
Rat Creatine Kinase Mb Ck Mb Elisa Kit, supplied by Cusabio, 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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Proteintech ckb
Figure 3. ISL treatment enhanced the expression of mitochondrial biogenesis and thermogenesis- related genes and proteins. (A) The mRNA levels of UCP1, <t>UCP2,</t> <t>PPARGC1a,</t> and PRDM16 in the BAT (n = 3). (B) Representative UCP1 staining of BAT (n = 3). (C,D) The protein levels of PPARGC1a, UCP1, and <t>CKB</t> in BAT (n = 3). * p < 0.05, ** p < 0.01.
Ckb, supplied by Proteintech, 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/product/creatine/CKB%2FCKM+Antibody/pm40004080-240-40-41
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Proteintech anti slc6a8
Figure 3. ISL treatment enhanced the expression of mitochondrial biogenesis and thermogenesis- related genes and proteins. (A) The mRNA levels of UCP1, <t>UCP2,</t> <t>PPARGC1a,</t> and PRDM16 in the BAT (n = 3). (B) Representative UCP1 staining of BAT (n = 3). (C,D) The protein levels of PPARGC1a, UCP1, and <t>CKB</t> in BAT (n = 3). * p < 0.05, ** p < 0.01.
Anti Slc6a8, supplied by Proteintech, 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 anti ckb antibody
Figure 3. ISL treatment enhanced the expression of mitochondrial biogenesis and thermogenesis- related genes and proteins. (A) The mRNA levels of UCP1, <t>UCP2,</t> <t>PPARGC1a,</t> and PRDM16 in the BAT (n = 3). (B) Representative UCP1 staining of BAT (n = 3). (C,D) The protein levels of PPARGC1a, UCP1, and <t>CKB</t> in BAT (n = 3). * p < 0.05, ** p < 0.01.
Anti Ckb 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
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Elabscience Biotechnology creatine kinase
Figure 3. ISL treatment enhanced the expression of mitochondrial biogenesis and thermogenesis- related genes and proteins. (A) The mRNA levels of UCP1, <t>UCP2,</t> <t>PPARGC1a,</t> and PRDM16 in the BAT (n = 3). (B) Representative UCP1 staining of BAT (n = 3). (C,D) The protein levels of PPARGC1a, UCP1, and <t>CKB</t> in BAT (n = 3). * p < 0.05, ** p < 0.01.
Creatine Kinase, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cusabio mouse ck mb enzyme linked immunosorbent assay elisa kit
Fig. 1. Effects of probiotics on body weight and cardiac function in myocardial injury model in sepsis mice Three groups were set: control (sham surgery), cecal ligation and puncture (CLP)-induced sepsis group, and CLP-induced sepsis plus probiotics (golden bifid) treatment group. Mice were randomly allocated into three groups and treated accordingly. (A) Mice weight was monitored on days 0, 2, and 4 of modeling. (B) The surviving hours of mice were analyzed using survival curves. (C) Cardiac functions were evaluated using Echocardiography. (D) Serum CK-MB release was determined using <t>ELISA.</t> (E) Histopathological alterations were evaluated using H&E staining. (F) Myocardial apoptosis was examined using TUNEL staining. (G-H) Cardiomyocyte size change was determined by WGA staining. (I) The protein levels of Bax, Bcl-2, and cleaved-caspase 3 using Immunoblotting. ** p < 0.01, vs. control group; ## p < 0.01, vs. CLP group.
Mouse Ck Mb Enzyme Linked Immunosorbent Assay Elisa Kit, supplied by Cusabio, 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 creatine kinase m b
Fig. 1. Effects of probiotics on body weight and cardiac function in myocardial injury model in sepsis mice Three groups were set: control (sham surgery), cecal ligation and puncture (CLP)-induced sepsis group, and CLP-induced sepsis plus probiotics (golden bifid) treatment group. Mice were randomly allocated into three groups and treated accordingly. (A) Mice weight was monitored on days 0, 2, and 4 of modeling. (B) The surviving hours of mice were analyzed using survival curves. (C) Cardiac functions were evaluated using Echocardiography. (D) Serum CK-MB release was determined using <t>ELISA.</t> (E) Histopathological alterations were evaluated using H&E staining. (F) Myocardial apoptosis was examined using TUNEL staining. (G-H) Cardiomyocyte size change was determined by WGA staining. (I) The protein levels of Bax, Bcl-2, and cleaved-caspase 3 using Immunoblotting. ** p < 0.01, vs. control group; ## p < 0.01, vs. CLP group.
Creatine Kinase M B, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Santa Cruz Biotechnology anti creatine kinase ck mb
Fig. 1. Effects of probiotics on body weight and cardiac function in myocardial injury model in sepsis mice Three groups were set: control (sham surgery), cecal ligation and puncture (CLP)-induced sepsis group, and CLP-induced sepsis plus probiotics (golden bifid) treatment group. Mice were randomly allocated into three groups and treated accordingly. (A) Mice weight was monitored on days 0, 2, and 4 of modeling. (B) The surviving hours of mice were analyzed using survival curves. (C) Cardiac functions were evaluated using Echocardiography. (D) Serum CK-MB release was determined using <t>ELISA.</t> (E) Histopathological alterations were evaluated using H&E staining. (F) Myocardial apoptosis was examined using TUNEL staining. (G-H) Cardiomyocyte size change was determined by WGA staining. (I) The protein levels of Bax, Bcl-2, and cleaved-caspase 3 using Immunoblotting. ** p < 0.01, vs. control group; ## p < 0.01, vs. CLP group.
Anti Creatine Kinase Ck Mb, 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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Elabscience Biotechnology ck mb
Fig. 1. Effects of probiotics on body weight and cardiac function in myocardial injury model in sepsis mice Three groups were set: control (sham surgery), cecal ligation and puncture (CLP)-induced sepsis group, and CLP-induced sepsis plus probiotics (golden bifid) treatment group. Mice were randomly allocated into three groups and treated accordingly. (A) Mice weight was monitored on days 0, 2, and 4 of modeling. (B) The surviving hours of mice were analyzed using survival curves. (C) Cardiac functions were evaluated using Echocardiography. (D) Serum CK-MB release was determined using <t>ELISA.</t> (E) Histopathological alterations were evaluated using H&E staining. (F) Myocardial apoptosis was examined using TUNEL staining. (G-H) Cardiomyocyte size change was determined by WGA staining. (I) The protein levels of Bax, Bcl-2, and cleaved-caspase 3 using Immunoblotting. ** p < 0.01, vs. control group; ## p < 0.01, vs. CLP group.
Ck Mb, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Figure 3. ISL treatment enhanced the expression of mitochondrial biogenesis and thermogenesis- related genes and proteins. (A) The mRNA levels of UCP1, UCP2, PPARGC1a, and PRDM16 in the BAT (n = 3). (B) Representative UCP1 staining of BAT (n = 3). (C,D) The protein levels of PPARGC1a, UCP1, and CKB in BAT (n = 3). * p < 0.05, ** p < 0.01.

Journal: International journal of molecular sciences

Article Title: Isoliquiritigenin Ameliorates High-Fat Diet-Induced Obesity in Mice by Activating Brown Adipose Tissue.

doi: 10.3390/ijms26041616

Figure Lengend Snippet: Figure 3. ISL treatment enhanced the expression of mitochondrial biogenesis and thermogenesis- related genes and proteins. (A) The mRNA levels of UCP1, UCP2, PPARGC1a, and PRDM16 in the BAT (n = 3). (B) Representative UCP1 staining of BAT (n = 3). (C,D) The protein levels of PPARGC1a, UCP1, and CKB in BAT (n = 3). * p < 0.05, ** p < 0.01.

Article Snippet: The following primary antibodies were used: C/EBPa (Proteintech, 18311-1-AP, 1:2000), FASN (Proteintech, 10624-2-AP, 1:5000), GLUT4 (Santa Cruz Biotechnology, Dallas, TX, USA, sc-53566, 1:2000), PPARG (Proteintech, 16643-1-AP, 1:2000), FABP4 (Proteintech, 12802- 1-AP, 1:6000), ATGL (Proteintech, 55190-1-AP, 1:2000), PPARGC1a (Proteintech, 66369-1-Ig, 1:6000), CKB (Proteintech, 15137-1-AP, 1:5000), UCP1 (Proteintech, 23673-1-AP, 1:2000), and GAPDH (Proteintech, 10494-1-AP, 1:5000).

Techniques: Expressing, Staining

Fig. 1. Effects of probiotics on body weight and cardiac function in myocardial injury model in sepsis mice Three groups were set: control (sham surgery), cecal ligation and puncture (CLP)-induced sepsis group, and CLP-induced sepsis plus probiotics (golden bifid) treatment group. Mice were randomly allocated into three groups and treated accordingly. (A) Mice weight was monitored on days 0, 2, and 4 of modeling. (B) The surviving hours of mice were analyzed using survival curves. (C) Cardiac functions were evaluated using Echocardiography. (D) Serum CK-MB release was determined using ELISA. (E) Histopathological alterations were evaluated using H&E staining. (F) Myocardial apoptosis was examined using TUNEL staining. (G-H) Cardiomyocyte size change was determined by WGA staining. (I) The protein levels of Bax, Bcl-2, and cleaved-caspase 3 using Immunoblotting. ** p < 0.01, vs. control group; ## p < 0.01, vs. CLP group.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Article Title: Golden bifid treatment regulates gut microbiota and serum metabolites to improve myocardial dysfunction in cecal ligation and puncture-induced sepsis mice.

doi: 10.1016/j.bbadis.2024.167049

Figure Lengend Snippet: Fig. 1. Effects of probiotics on body weight and cardiac function in myocardial injury model in sepsis mice Three groups were set: control (sham surgery), cecal ligation and puncture (CLP)-induced sepsis group, and CLP-induced sepsis plus probiotics (golden bifid) treatment group. Mice were randomly allocated into three groups and treated accordingly. (A) Mice weight was monitored on days 0, 2, and 4 of modeling. (B) The surviving hours of mice were analyzed using survival curves. (C) Cardiac functions were evaluated using Echocardiography. (D) Serum CK-MB release was determined using ELISA. (E) Histopathological alterations were evaluated using H&E staining. (F) Myocardial apoptosis was examined using TUNEL staining. (G-H) Cardiomyocyte size change was determined by WGA staining. (I) The protein levels of Bax, Bcl-2, and cleaved-caspase 3 using Immunoblotting. ** p < 0.01, vs. control group; ## p < 0.01, vs. CLP group.

Article Snippet: The CK-MB concentration within the serum was measured using the Mouse CK-MB enzyme-linked immunosorbent assay (ELISA) kit (CSBE14404m, CUSABIO, China).

Techniques: Probiotics, Control, Ligation, Enzyme-linked Immunosorbent Assay, Staining, TUNEL Assay, Western Blot

Fig. 2. Effects of probiotics on inflammatory and oxidative stress-related indicators in myocardial injury model in sepsis mice (A) The levels of TNF-α, IL-1β, and IL-6 in myocardial tissues were examined using ELISA. (B) The levels of TNF-α, IL-1β, and IL-6 in mice serum were examined using ELISA. (C) The protein levels of SOD were examined using Immunoblotting. (D) The activity of SOD was determined using ELISA. (E) The levels of oxidative damage marker 8-OHdG were determined using ELISA. ** p < 0.01, vs. control group; # p < 0.05, ## p < 0.01, vs. CLP group.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Article Title: Golden bifid treatment regulates gut microbiota and serum metabolites to improve myocardial dysfunction in cecal ligation and puncture-induced sepsis mice.

doi: 10.1016/j.bbadis.2024.167049

Figure Lengend Snippet: Fig. 2. Effects of probiotics on inflammatory and oxidative stress-related indicators in myocardial injury model in sepsis mice (A) The levels of TNF-α, IL-1β, and IL-6 in myocardial tissues were examined using ELISA. (B) The levels of TNF-α, IL-1β, and IL-6 in mice serum were examined using ELISA. (C) The protein levels of SOD were examined using Immunoblotting. (D) The activity of SOD was determined using ELISA. (E) The levels of oxidative damage marker 8-OHdG were determined using ELISA. ** p < 0.01, vs. control group; # p < 0.05, ## p < 0.01, vs. CLP group.

Article Snippet: The CK-MB concentration within the serum was measured using the Mouse CK-MB enzyme-linked immunosorbent assay (ELISA) kit (CSBE14404m, CUSABIO, China).

Techniques: Probiotics, Enzyme-linked Immunosorbent Assay, Western Blot, Activity Assay, Marker, Control

Fig. 3. Effects of probiotics on intestinal mucosal permeability and barrier function in myocardial injury model in sepsis mice (A) The intestinal mucous layer thickness was determined using Alcian blue staining. (B) The levels of LPS in serum were determined using ELISA. (C) The levels and distribution of tight junction protein ZO-1 and occludin were detected by Immunofluorescence staining (IF). ** p < 0.01, vs. control group; # p < 0.05, vs. CLP group.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Article Title: Golden bifid treatment regulates gut microbiota and serum metabolites to improve myocardial dysfunction in cecal ligation and puncture-induced sepsis mice.

doi: 10.1016/j.bbadis.2024.167049

Figure Lengend Snippet: Fig. 3. Effects of probiotics on intestinal mucosal permeability and barrier function in myocardial injury model in sepsis mice (A) The intestinal mucous layer thickness was determined using Alcian blue staining. (B) The levels of LPS in serum were determined using ELISA. (C) The levels and distribution of tight junction protein ZO-1 and occludin were detected by Immunofluorescence staining (IF). ** p < 0.01, vs. control group; # p < 0.05, vs. CLP group.

Article Snippet: The CK-MB concentration within the serum was measured using the Mouse CK-MB enzyme-linked immunosorbent assay (ELISA) kit (CSBE14404m, CUSABIO, China).

Techniques: Probiotics, Permeability, Staining, Enzyme-linked Immunosorbent Assay, Immunofluorescence, IF-P, Control