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rabbit anti mat1a  (Proteintech)


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    Proteintech rabbit anti mat1a
    Rabbit Anti Mat1a, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 17 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+mat1a/MAT1A+Antibody/pm38713722-485-43-47
    Average 93 stars, based on 17 article reviews
    rabbit anti mat1a - by Bioz Stars, 2026-11
    93/100 stars

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    Related Articles

    Western Blot:

    Article Title: Antibiotic-Induced Gut Microbiota Dysbiosis Modulates Host Transcriptome and m 6 A Epitranscriptome via Bile Acid Metabolism.
    Article Snippet: Gut microbiota can influence host gene expression and physiology through metabolites.. Besides, the presence or absence of gut microbiome can reprogram host transcriptome and epitranscriptome as represented by N6-methyladenosine (m6A), the most abundant mammalian mRNA modification.. However, which and how gut microbiota-derived metabolites reprogram host transcriptome and m6A epitranscriptome remain poorly understood.

    Immunofluorescence:

    Article Title: Antibiotic-Induced Gut Microbiota Dysbiosis Modulates Host Transcriptome and m 6 A Epitranscriptome via Bile Acid Metabolism.
    Article Snippet: Gut microbiota can influence host gene expression and physiology through metabolites.. Besides, the presence or absence of gut microbiome can reprogram host transcriptome and epitranscriptome as represented by N6-methyladenosine (m6A), the most abundant mammalian mRNA modification.. However, which and how gut microbiota-derived metabolites reprogram host transcriptome and m6A epitranscriptome remain poorly understood.



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    FIG. 7. Effects of BPA on expression of <t>Mat1a</t> and Mat2a genes and SAMe in the liver. (A) Effects of BPA on mRNA levels of Mat1a and Mat2a genes in rat liver. Each bar represents the mean ± SEM, n = 6 for each group. The data shown are representative of the results of three independent RT-PCR analysis. Each value was normalized to the mRNA expression of Gapdh, and summary of results is expressed as percentage of control mRNA levels. V, vehicle control group; L, low-dose group (0.5 g/kg/day); H, high-dose group (50 mg/kg/day). Significance level: **p < 0.05 compared with controls. (B) Effects of BPA on the expression of hepatic proteins of MAT1A and MAT2A. Representative western blots show expression of MAT1A (left) and MAT2A (right) and corresponding GAPDH. The lower trace of each panel shows the bar graph summarizing the immunoblot data. Densitometric results are expressed as mean ± SEM (n = 6 for each group). Each value was normalized to GAPDH, and the relative expression levels were generated compared with the control value. Significance level: **p < 0.05 compared with controls. (C) Effects of BPA on hepatic SAMe levels. Results are expressed as mean ± SEM (n = 6 for each group) and percentage of control SAMe levels. Significance level: **p < 0.05 compared with controls.
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    FIG. 7. Effects of BPA on expression of Mat1a and Mat2a genes and SAMe in the liver. (A) Effects of BPA on mRNA levels of Mat1a and Mat2a genes in rat liver. Each bar represents the mean ± SEM, n = 6 for each group. The data shown are representative of the results of three independent RT-PCR analysis. Each value was normalized to the mRNA expression of Gapdh, and summary of results is expressed as percentage of control mRNA levels. V, vehicle control group; L, low-dose group (0.5 g/kg/day); H, high-dose group (50 mg/kg/day). Significance level: **p < 0.05 compared with controls. (B) Effects of BPA on the expression of hepatic proteins of MAT1A and MAT2A. Representative western blots show expression of MAT1A (left) and MAT2A (right) and corresponding GAPDH. The lower trace of each panel shows the bar graph summarizing the immunoblot data. Densitometric results are expressed as mean ± SEM (n = 6 for each group). Each value was normalized to GAPDH, and the relative expression levels were generated compared with the control value. Significance level: **p < 0.05 compared with controls. (C) Effects of BPA on hepatic SAMe levels. Results are expressed as mean ± SEM (n = 6 for each group) and percentage of control SAMe levels. Significance level: **p < 0.05 compared with controls.

    Journal: Toxicological sciences : an official journal of the Society of Toxicology

    Article Title: Metabolomic analysis reveals metabolic changes caused by bisphenol A in rats.

    doi: 10.1093/toxsci/kfu016

    Figure Lengend Snippet: FIG. 7. Effects of BPA on expression of Mat1a and Mat2a genes and SAMe in the liver. (A) Effects of BPA on mRNA levels of Mat1a and Mat2a genes in rat liver. Each bar represents the mean ± SEM, n = 6 for each group. The data shown are representative of the results of three independent RT-PCR analysis. Each value was normalized to the mRNA expression of Gapdh, and summary of results is expressed as percentage of control mRNA levels. V, vehicle control group; L, low-dose group (0.5 g/kg/day); H, high-dose group (50 mg/kg/day). Significance level: **p < 0.05 compared with controls. (B) Effects of BPA on the expression of hepatic proteins of MAT1A and MAT2A. Representative western blots show expression of MAT1A (left) and MAT2A (right) and corresponding GAPDH. The lower trace of each panel shows the bar graph summarizing the immunoblot data. Densitometric results are expressed as mean ± SEM (n = 6 for each group). Each value was normalized to GAPDH, and the relative expression levels were generated compared with the control value. Significance level: **p < 0.05 compared with controls. (C) Effects of BPA on hepatic SAMe levels. Results are expressed as mean ± SEM (n = 6 for each group) and percentage of control SAMe levels. Significance level: **p < 0.05 compared with controls.

    Article Snippet: The membranes were incubated in blocking buffer for 2 h at room temperature, followed by overnight incubation at 4◦C with rabbit polyclonal antibodies for MAT1A (Proteintech Group Inc, Chicago, IL, 1:2000 dilution) and MAT2A (Beijing Biosynthesis Biotechnology CO., Ltd, Beijing, China, 1:500 dilution), and mouse polyclonal antibodies for GAPDH (Beyotime, China, 1:1000 dilution).

    Techniques: Expressing, Reverse Transcription Polymerase Chain Reaction, Control, Western Blot, Generated