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Acetyl-CoA Carboxylase 1 antibody

GTX132081
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetACACA
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Overview

  • Supplier
    GeneTex
  • Product Name
    Acetyl-CoA Carboxylase 1 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1.55 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID31
  • Target name
    ACACA
  • Target description
    acetyl-CoA carboxylase alpha
  • Target synonyms
    ACAC, ACACAD, ACACalpha, ACC, ACC1, ACCA, ACCalpha, Acac1, hACC1, acetyl-CoA carboxylase 1, ACC-alpha, acetyl-Coenzyme A carboxylase alpha
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ13085
  • Protein Name
    Acetyl-CoA carboxylase 1
  • Scientific Description
    Acetyl-CoA carboxylase (ACC) is a complex multifunctional enzyme system. ACC is a biotin-containing enzyme which catalyzes the carboxylation of acetyl-CoA to malonyl-CoA, the rate-limiting step in fatty acid synthesis. There are two ACC forms, alpha and beta, encoded by two different genes. ACC-alpha is highly enriched in lipogenic tissues. The enzyme is under long term control at the transcriptional and translational levels and under short term regulation by the phosphorylation/dephosphorylation of targeted serine residues and by allosteric transformation by citrate or palmitoyl-CoA. Multiple alternatively spliced transcript variants divergent in the 5 sequence and encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Huang YC, Hou MF, Tsai YM, et al. Involvement of ACACA (acetyl-CoA carboxylase α) in the lung pre-metastatic niche formation in breast cancer by senescence phenotypic conversion in fibroblasts. Cell Oncol (Dordr). 2023,46(3):643-660. doi: 10.1007/s13402-022-00767-5
    Read this paper
  • Ceja-Galicia ZA, García-Arroyo FE, Aparicio-Trejo OE, et al. Therapeutic Effect of Curcumin on 5/6Nx Hypertriglyceridemia: Association with the Improvement of Renal Mitochondrial β-Oxidation and Lipid Metabolism in Kidney and Liver. Antioxidants (Basel). 2022,11(11). doi: 10.3390/antiox11112195
    Read this paper
  • Chang TC, Chiou WC, Lai WH, et al. Ugonin J improves metabolic disorder and ameliorates nonalcoholic fatty liver disease by regulating the AMPK/AKT signaling pathway. Pharmacol Res. 2021,163:105298. doi: 10.1016/j.phrs.2020.105298
    Read this paper
  • Tsai YT, Ruan JW, Chang CS, et al. Antrodia cinnamomea Confers Obesity Resistance and Restores Intestinal Barrier Integrity in Leptin-deficient Obese Mice. Nutrients. 2020,12(3). doi: 10.3390/nu12030726
    Read this paper
  • Chang TC, Chiang H, Lai YH, et al. Helminthostachys zeylanica alleviates hepatic steatosis and insulin resistance in diet-induced obese mice. BMC Complement Altern Med. 2019,19(1):368. doi: 10.1186/s12906-019-2782-3
    Read this paper
  • García-Arroyo FE, Monroy-Sánchez F, Muñoz-Jiménez I, et al. Allopurinol Prevents the Lipogenic Response Induced by an Acute Oral Fructose Challenge in Short-Term Fructose Fed Rats. Biomolecules. 2019,9(10). doi: 10.3390/biom9100601
    Read this paper
  • Liu HK, Hung TM, Huang HC, et al. Bai-Hu-Jia-Ren-Shen-Tang Decoction Reduces Fatty Liver by Activating AMP-Activated Protein Kinase In Vitro and In Vivo. Evid Based Complement Alternat Med. 2015,2015:651734. doi: 10.1155/2015/651734
    Read this paper
  • Jhuang HJ, Hsu WH, Lin KT, et al. Gluconeogenesis, lipogenesis, and HBV replication are commonly regulated by PGC-1α-dependent pathway. Oncotarget. 2015,6(10):7788-803.
    Read this paper