ACACB polyclonal antibody

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Specifications
Product Description
Goat polyclonal antibody raised against synthetic peptide of ACACB.
Immunogen
A synthetic peptide corresponding to human ACACB.
Sequence
C-QLGEPDLSDKDRKD
Host
Goat
Theoretical MW (kDa)
277
Form
Liquid
Purification
Antigen affinity purification
Concentration
0.5 mg/mL
Quality Control Testing
Antibody Reactive Against Synthetic Peptide.
Recommend Usage
ELISA (1:32000)
The optimal working dilution should be determined by the end user.Storage Buffer
In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
Storage Instruction
Store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Enzyme-linked Immunoabsorbent Assay
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Gene Info — ACACB
Entrez GeneID
32Protein Accession#
NP_001084.2Gene Name
ACACB
Gene Alias
ACC2, ACCB, HACC275
Gene Description
acetyl-Coenzyme A carboxylase beta
Omim ID
601557Gene Ontology
HyperlinkGene Summary
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. ACC-beta is thought to control fatty acid oxidation by means of the ability of malonyl-CoA to inhibit carnitine-palmitoyl-CoA transferase I, the rate-limiting step in fatty acid uptake and oxidation by mitochondria. ACC-beta may be involved in the regulation of fatty acid oxidation, rather than fatty acid biosynthesis. There is evidence for the presence of two ACC-beta isoforms. [provided by RefSeq
Other Designations
acetyl-CoA carboxylase 2
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Interactomes
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Pathways
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Diseases
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Publication Reference
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Aging-associated reductions in AMP-activated protein kinase activity and mitochondrial biogenesis.
Reznick RM, Zong H, Li J, Morino K, Moore IK, Yu HJ, Liu ZX, Dong J, Mustard KJ, Hawley SA, Befroy D, Pypaert M, Hardie DG, Young LH, Shulman GI.
Cell Metabolism 2007 Feb; 5(2):151.
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Aging-associated reductions in AMP-activated protein kinase activity and mitochondrial biogenesis.
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