ALDH3B2 polyclonal, anti-human, mouse, rat
€305.00
In stock
SKU
BS60095
Background:
ALDH3B2 (aldehyde dehydrogenase 3 family, member B2), also known as ALDH8, is a 385 amino acid protein that belongs to the ALDH family and is involved in the pathway of alcohol metabolism. Expressed in salivary gland tissue, ALDH3B2 functions to catalyze the NADP+-dependent conversion of an aldehyde into an acid. The gene encoding ALDH3B2 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
Alternative Name:
Aldehyde dehydrogenase family 3 member B2, Aldehyde dehydrogenase 8, ALDH3B2, ALDH8
Application Dilution: WB: 1:500~1:1000, IHC: 1:50~1:200
Specificity: ALDH3B2 polyclonal antibody detects endogenous levels of ALDH3B2 protein.
Immunogen:
A synthetic peptide corresponding to residues in Human ALDH3B2.
MW: ~ 43 kDa
Swis Prot.: P48448
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1 mg/ml in Phosphate buffered saline (PBS) with 0.05% sodium azide, approx. pH 7.2.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
ALDH3B2 (aldehyde dehydrogenase 3 family, member B2), also known as ALDH8, is a 385 amino acid protein that belongs to the ALDH family and is involved in the pathway of alcohol metabolism. Expressed in salivary gland tissue, ALDH3B2 functions to catalyze the NADP+-dependent conversion of an aldehyde into an acid. The gene encoding ALDH3B2 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
Alternative Name:
Aldehyde dehydrogenase family 3 member B2, Aldehyde dehydrogenase 8, ALDH3B2, ALDH8
Application Dilution: WB: 1:500~1:1000, IHC: 1:50~1:200
Specificity: ALDH3B2 polyclonal antibody detects endogenous levels of ALDH3B2 protein.
Immunogen:
A synthetic peptide corresponding to residues in Human ALDH3B2.
MW: ~ 43 kDa
Swis Prot.: P48448
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1 mg/ml in Phosphate buffered saline (PBS) with 0.05% sodium azide, approx. pH 7.2.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
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