ACAT1 polyclonal antibody
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Specification
Product Description
Rabbit polyclonal antibody raised against partial recombinant human ACAT1.
Immunogen
Recombinant protein corresponding to human ACAT1.
Sequence
VSATRTPIGSFLGSLSLLPATKLGSIAIQGAIEKAGIPKEEVKEAYMGNVLQGGEGQAPTRQAVLGAGLPISTPCTTINKVCASGMKAIMMASQSLMCGHQDVMVAGGMESMSNVPYVMNRGSTPYGGVKLEDLIVKDGLTD
Host
Rabbit
Reactivity
Human, Mouse, Rat
Form
Liquid
Purification
Antigen affinity purification
Isotype
IgG
Recommend Usage
Immunofluorescence (1-4 ug/mL)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1:50-1:200)
Western Blot (1:100-1:250)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH 7.2 (40% glycerol, 0.02% sodium azide).
Storage Instruction
Store at 4°C. For long term storage 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
Western Blot (Cell lysate)
Western Blot analysis of Lane 1: NIH-3T3 cell lysate (mouse embryonic fibroblast cells) and Lane 2: NBT-II cell lysate (Wistar rat bladder tumor cells) with ACAT1 polyclonal antibody (Cat # PAB30691).Western Blot
Western Blot analysis of Lane 1: RT-4, Lane 2: U-251MG sp, Lane 3: human plasma (IgG/HSA depleted), Lane 4: human liver and Lane 5: human tonsil lysates with ACAT1 polyclonal antibody (Cat # PAB30691).Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human liver with ACAT1 polyclonal antibody (Cat # PAB30691) shows strong cytoplasmic positivity in hepatocytes.Immunofluorescence
Immunofluorescent staining of A-431 cells with ACAT1 polyclonal antibody (Cat # PAB30691) (Green) shows positivity in mitochondria. -
Gene Info — ACAT1
Entrez GeneID
38Protein Accession#
P24752Gene Name
ACAT1
Gene Alias
ACAT, MAT, T2, THIL
Gene Description
acetyl-Coenzyme A acetyltransferase 1
Gene Ontology
HyperlinkGene Summary
This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq
Other Designations
acetoacetyl Coenzyme A thiolase
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Interactome
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Pathway
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Disease
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