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ACCα (K86) polyclonal antibody BS1377
  • Western blot (WB) analysis of ACCα (K86) polyclonal antibody at 1:500 dilution Lane1:Hela cell lysate Lane2:Jurkat cell lysate Lane3:NIH-3T3 cell lysate Lane4:PC12 cell lysate
  • Immunohistochemistry (IHC) analyzes of ACCα (K86) pAb in paraffin-embeddedhuman stomach carcinoma tissue at 1:50.showing cell membrane, cytoplasmicstaining. Negative control (the right)Using PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG-biotin followed by avidin-peroxidase.
Product NameACCα (K86) polyclonal antibody
Catalog No.BS1377
Swiss-ProtQ13085
Host Rabbit
ReactivityHuman,Mouse,Rat,Pig
ApplicationsWB IHC
Application_allWB: 1:500~1:1000 IHC: 1:50~1:200
BiowMW~ 265 kDa
Alternative NameAcetyl-CoA carboxylase 1; Short name=ACC1; ACC-alpha; Biotin carboxylase; ACACA; ACAC; ACC1; ACCA
Purification&PurityThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
ConjugateUnconjugated
ModificationUnmodification
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Size Price
50ul $158
100ul $275
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Product Name :
ACCα (K86) polyclonal antibody
Background :
Acetyl-CoA carboxylase (ACC) is a complex multifunctional enzyme system which catalyzes the carboxylation of acetyl-CoA to malonyl-CoA, the ratelimiting step in fatty acid synthesis. Exercise diminishes the activity of acetyl- CoA carboxylase in human muscle. ACCα (ACC1) is the rate-limiting enzyme in the biogenesis of long-chain fatty acids, and ACCβ (ACC2) may control mitochondrial fatty acid oxidation. These two isoforms of ACC control the amount of fatty acids in the cells. The catalytic function of ACCα is regulated by phosphorylation (inactive) and dephosphorylation (active) of targeted Serine residues and by allosteric transformation by citrate or palmitoyl-CoA, which serve as the short-term regulatory mechanism of the enzyme. The gene encoding ACCα, which maps to human chromosome 17, encodes the 265 kDa α form of ACC, which is the major ACC in lipogenic tissues. The catalytic core of ACCβ is homologous to that of ACCα except for an additional peptide of about 150 amino acids at the N-terminus.
Product :
Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2
Storage&Stability :
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
Specificity :
ACCα (H74) polyclonal antibody detects endogenous levels of ACCα protein.
Immunogen :
Synthetic peptide, corresponding to amino acids 50-100 of Human ACCα.
Conjugate :
Unconjugated
Modification :
Unmodification
  • Western blot (WB) analysis of ACCα (K86) polyclonal antibody at 1:500 dilution Lane1:Hela cell lysate Lane2:Jurkat cell lysate Lane3:NIH-3T3 cell lysate Lane4:PC12 cell lysate
  • Immunohistochemistry (IHC) analyzes of ACCα (K86) pAb in paraffin-embeddedhuman stomach carcinoma tissue at 1:50.showing cell membrane, cytoplasmicstaining. Negative control (the right)Using PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG-biotin followed by avidin-peroxidase.
Madecassic acid, the contributor to the anti-colitis effect of madecassoside, enhances the shift of Th17 toward Treg cells via the PPARγ/AMPK/ACC1 pathway PMCID:    Pubmed No.:28358365 Ilexgenin A inhibits endoplasmic reticulum stress and ameliorates endothelial dysfunction via suppression of TXNIP/NLRP3 inflammasome activation in an AMPK dependent manner. PMCID:    Pubmed No.:26054569 Lipopolysaccharide significantly influences the hepatic triglyceride metabolism in growing pigs PMCID:    Pubmed No.:26121977 Inhibition of Mitochondrial Fission and NOX2 Expression Prevent NLRP3 Inflammasome Activation in the Endothelium: The Role of Corosolic Acid Action in the Amelioration of Endothelial Dysfunction PMCID:    Pubmed No.:26869350 Ilexgenin A inhibits endoplasmic reticulum stress and ameliorates endothelial dysfunction via suppression of TXNIP/NLRP3 inflammasome activation in an AMPK dependent manner PMCID:    Pubmed No.:26054569 d‐Chiro inositol ameliorates endothelial dysfunction via inhibition of oxidative stress and mitochondrial fission PMCID:    Pubmed No.:28087886 Mangiferin suppresses endoplasmic reticulum stress in perivascular adipose tissue and prevents insulin resistance in the endothelium PMCID:    Pubmed No.:30666402 Inhibition of lipolysis by ilexgenin A via AMPK activation contributes to the prevention of hepatic insulin resistance PMCID:    Pubmed No.:28739087 Vanadium(IV)-chlorodipicolinate inhibits 3T3-L1 preadipocyte adipogenesis by activating LKB1/AMPK signaling pathway PMCID:    Pubmed No.:27318173 Lipopolysaccharide significantly influences the hepatic triglyceride metabolism in growing pigs PMCID:    Pubmed No.:26121977 HSPA12A is required for adipocyte differentiation and diet-induced obesity through a positive feedback regulation with PPARγ PMCID:    Pubmed No.:30742088 SOCS2 Inhibits Mitochondrial Fatty Acid Oxidation via Suppressing LepR/JAK2/AMPK Signaling Pathway in Mouse Adipocytes PMCID:    Pubmed No.:32733634 Adipokine zinc-α2-glycoprotein alleviates lipopolysaccharide-induced inflammatory responses through the β3-AR/PKA/CREB pathway PMCID:    Pubmed No.:31260855
Bioworld Biotech only provide peptides for our antibodies and do not provide additional peptide customization services.

Price/Size :

USD 368/1mg/vial



Tips: 

For phospho antibody, we provide phospho peptide(0.5mg) and non-phospho peptide(0.5mg).

Describe :

Blocking peptides are peptides that bind specifically to the target antibody and block antibody binding. These peptide usually contains the epitope recognized by the antibody. Antibodies bound to the blocking peptide no longer bind to the epitope on the target protein. This mechanism is useful when non-specific binding is an issue, for example, in Western blotting (WB) and Immunohistochemistry (IHC). By comparing the staining from the blocked antibody versus the antibody alone, one can see which staining is specific; Specific binding will be absent from the western blot or IHC performed with the neutralized antibody.

Formula:

Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 10 mg/ml.The purity is >90%,tested by HPLC and MS.

Storage:

The freeze-dried powder is more stable. For short time at 2-8°C. For long term storage store at -20°C. 


Note :

This product is for research use only (RUO only). Not for use in diagnostic or therapeutic procedures.
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