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NSJ Bioreagents

SKU:R32489

ABHD5 Antibody / CGI-58

ABHD5 Antibody / CGI-58

Regular price $449.00 USD
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1-acylglycerol-3-phosphate O-acyltransferase ABHD5 is an enzyme that in humans is encoded by the ABHD5 gene. The protein encoded by this gene belongs to a large family of proteins defined by an alpha/beta hydrolase fold, and contains three sequence motifs that correspond to a catalytic triad found in the esterase/lipase/thioesterase subfamily. It differs from other members of this subfamily in that its putative catalytic triad contains an asparagine instead of the serine residue. Mutations in this gene have been associated withChanarin-Dorfman syndrome, a triglyceride storage disease with impaired long-chain fatty acid oxidation.

Specifications

Family Primary antibody
Formulation 0.5mg/ml if reconstituted with 0.2ml sterile DI water
Format Antigen affinity purified
Host Animal Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit IgG
Species Reactivity Human, Rat
Application WB, IHC-P, IF/ICC
Application Details Western blot: 0.5-1ug/ml,IHC (FFPE): 1-2ug/ml,IF/ICC (FFPE): 2-4ug/ml
Application Note Differences in protocols and secondary/substrate sensitivity may require the ABHD5 antibody to be titrated for optimal performance.
Localization Cytoplasmic
Immunogen Amino acids R169-D349 from the human protein were used as the immunogen for the ABHD5 antibody.
Buffer Lyophilized from 1X PBS with 2.5% BSA and 0.025% sodium azide
Purity Antigen affinity
Storage After reconstitution, the ABHD5 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
Limitation This ABHD5 antibody is available for research use only.
Uniprot # Q8WTS1
Status Available
PDF Link https://www.nsjbio.com/tds-pdf/abhd5-antibody-cgi-58-r32489
Title ABHD5 Antibody / CGI-58
Description 1-acylglycerol-3-phosphate O-acyltransferase ABHD5 is an enzyme that in humans is encoded by the ABHD5 gene. The protein encoded by this gene belongs to a large family of proteins defined by an alpha/beta hydrolase fold, and contains three sequence motifs that correspond to a catalytic triad found in the esterase/lipase/thioesterase subfamily. It differs from other members of this subfamily in that its putative catalytic triad contains an asparagine instead of the serine residue. Mutations in this gene have been associated withChanarin-Dorfman syndrome, a triglyceride storage disease with impaired long-chain fatty acid oxidation.
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