GLA polyclonal (N-term), anti-human

GLA polyclonal (N-term), anti-human

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In stock
SKU
AC-AP6727A
Catalog Number: AC-AP6727A
Size: 80 µl, 400 µl
Isotype: Rabbit IgG
Clone Name: RB19115
Applications: FC, IF, IHC-P, WB
Datasheet

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Background:
GLA is a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties.

Other Names:
Alpha-galactosidase A, Alpha-D-galactosidase A, Alpha-D-galactoside galactohydrolase, Melibiase, Agalsidase, GLA

Target/Specificity:
This GLA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 83-112 amino acids from the N-terminal region of human GLA.

Antigen Region:
83-112

Antigen Type: Synthetic Peptide

Gene Name: GLA (HGNC:4296)
Gene ID: 2717
Primary Accession: P06280
NCBI Accession: NP_000160.1
Format: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
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