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ast c010 2 1  (Elabscience Biotechnology)


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    Elabscience Biotechnology ast c010 2 1
    Ast C010 2 1, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 166 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ast+c010+2+1/Creatinine+(Cr)+Colorimetric+Assay+Kit/pm41790377-120-45-60
    Average 96 stars, based on 166 article reviews
    ast c010 2 1 - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    AST Assay:

    Article Title: Tu-Si-Zi-Wan reduces D-galactose-induced hepatic and cerebral oxidative damage in aging mice via the Nrf2/ARE pathway
    Article Snippet: .. Serum was obtained by centrifuging whole blood samples at 4 °C and 3000 rpm for 10 min. Assays were performed strictly according to the manufacturers’ instructions: ALT (Cat. No. C009-2-1) and AST (Cat. No. C010-2-1) from Nanjing Jiancheng Bioengineering Institute (Nanjing, China); TG (Cat. No. E-BC-K261-M), TC (Cat. No. E-BC-K109-M), Cr (Cat. No. E-BC-K188-M), and Urea (Cat. No. E-BC-K183-M) from Elabscience Biotechnology Co., Ltd., (Wuhan, China). .. The absorbance was measured via a Bio-Rad microplate reader (Hercules, CA, USA), and the concentrations were determined on the basis of standard curves.

    Article Title: Tu-Si-Zi-Wan reduces D-galactose-induced hepatic and cerebral oxidative damage in aging mice via the Nrf2/ARE pathway.
    Article Snippet: .. Serum was obtained by centrifuging whole blood samples at 4 °C and 3000 rpm for 10 min. Assays were performed strictly according to the manufacturers’ instructions: ALT (Cat. No. C009-2-1) and AST (Cat. No. C010-2-1) from Nanjing Jiancheng Bioengineering Institute (Nanjing, China); TG (Cat. No. E-BC-K261-M), TC (Cat. No. E-BC-K109-M), Cr (Cat. No. E-BC-K188-M), and Urea (Cat. No. E-BC-K183-M) from Elabscience Biotechnology Co., Ltd., (Wuhan, China). .. The absorbance was measured via a Bio-Rad microplate reader (Hercules, CA, USA), and the concentrations were determined on the basis of standard curves.



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    (A-J) Male control and Mtarc1 null mice (MKO) were challenged with CDAHFD for eight weeks and sacrificed for phenotyping (n = 9-10/group). (A) Animal diet challenge experiment workflow. (B) Liver body weight ratio (%). (C) Hepatic TG content. (D) Representative images of livers subjected to Oil Red O staining and H&E staining (Scale bar, 100 μm). (E) Activity of serum alanine <t>aminotransferase</t> (ALT). (F) Activity of serum aspartate aminotransferase <t>(AST).</t> (G) Serum total-bilirubin level. (H) Hepatic qPCR assay for genes as indicated. (I) Immunoblotting for COL1A1 and quantification. (J) Representative images of liver sections subjected to Sirius Red staining (Scale bar, 100 μm). (K-P) Female control and MKO mice were challenged with CDAHFD for eight weeks and sacrificed for phenotyping (n = 10/group). (K) Liver body weight ratio (%). (L) Hepatic TG content. (M) Activity of serum ALT. (N) Activity of serum AST. (O) Serum total-bilirubin level. (P) Hepatic qPCR assay for genes as indicated. Data were expressed as mean ± SEM and analyzed by Student’s t-test. * p < 0.05, ** p < 0.01.
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    Image Search Results


    (A-J) Male control and Mtarc1 null mice (MKO) were challenged with CDAHFD for eight weeks and sacrificed for phenotyping (n = 9-10/group). (A) Animal diet challenge experiment workflow. (B) Liver body weight ratio (%). (C) Hepatic TG content. (D) Representative images of livers subjected to Oil Red O staining and H&E staining (Scale bar, 100 μm). (E) Activity of serum alanine aminotransferase (ALT). (F) Activity of serum aspartate aminotransferase (AST). (G) Serum total-bilirubin level. (H) Hepatic qPCR assay for genes as indicated. (I) Immunoblotting for COL1A1 and quantification. (J) Representative images of liver sections subjected to Sirius Red staining (Scale bar, 100 μm). (K-P) Female control and MKO mice were challenged with CDAHFD for eight weeks and sacrificed for phenotyping (n = 10/group). (K) Liver body weight ratio (%). (L) Hepatic TG content. (M) Activity of serum ALT. (N) Activity of serum AST. (O) Serum total-bilirubin level. (P) Hepatic qPCR assay for genes as indicated. Data were expressed as mean ± SEM and analyzed by Student’s t-test. * p < 0.05, ** p < 0.01.

    Journal: bioRxiv

    Article Title: MTARC1 Regulates Lipid Droplet Degradation via Phospholipid Remodeling in Metabolic Fatty Liver Disease

    doi: 10.1101/2025.07.17.665462

    Figure Lengend Snippet: (A-J) Male control and Mtarc1 null mice (MKO) were challenged with CDAHFD for eight weeks and sacrificed for phenotyping (n = 9-10/group). (A) Animal diet challenge experiment workflow. (B) Liver body weight ratio (%). (C) Hepatic TG content. (D) Representative images of livers subjected to Oil Red O staining and H&E staining (Scale bar, 100 μm). (E) Activity of serum alanine aminotransferase (ALT). (F) Activity of serum aspartate aminotransferase (AST). (G) Serum total-bilirubin level. (H) Hepatic qPCR assay for genes as indicated. (I) Immunoblotting for COL1A1 and quantification. (J) Representative images of liver sections subjected to Sirius Red staining (Scale bar, 100 μm). (K-P) Female control and MKO mice were challenged with CDAHFD for eight weeks and sacrificed for phenotyping (n = 10/group). (K) Liver body weight ratio (%). (L) Hepatic TG content. (M) Activity of serum ALT. (N) Activity of serum AST. (O) Serum total-bilirubin level. (P) Hepatic qPCR assay for genes as indicated. Data were expressed as mean ± SEM and analyzed by Student’s t-test. * p < 0.05, ** p < 0.01.

    Article Snippet: Serum TG (Jiancheng, A110-1-1), total cholesterol (Jiancheng, A111-1-1), glucose (Jiancheng, A154-1-1), non-esterified fatty acid (NEFA) (Jiancheng, A042-2-1), alanine aminotransferase (ALT) (Jiancheng, C009-2-1), aspartate aminotransferase (AST) (Jiancheng, C010-2-1), and total-bilirubin levels (SolarBio, BC5185) were measured according to the instructions provided by the manufacturers, with some assay performed using an automated biochemical analyzer (Mindary, China).

    Techniques: Control, Staining, Activity Assay, Western Blot