GLA purified MaxPab rabbit polyclonal antibody (D01P)
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More Files
- More Functions
Western Blot (Cell lysate)
GLA MaxPab rabbit polyclonal antibody. Western Blot analysis of GLA expression in HeLa.
Western Blot (Transfected lysate)
Western Blot analysis of GLA expression in transfected 293T cell line (H00002717-T02) by GLA MaxPab polyclonal antibody.
Lane 1: GLA transfected lysate(48.80 KDa).
Lane 2: Non-transfected lysate.
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Specification
Product Description
Rabbit polyclonal antibody raised against a full-length human GLA protein.
Immunogen
GLA (NP_000160.1, 1 a.a. ~ 429 a.a) full-length human protein.
Sequence
MQLRNPELHLGCALALRFLALVSWDIPGARALDNGLARTPTMGWLHWERFMCNLDCQEEPDSCISEKLFMEMAELMVSEGWKDAGYEYLCIDDCWMAPQRDSEGRLQADPQRFPHGIRQLANYVHSKGLKLGIYADVGNKTCAGFPGSFGYYDIDAQTFADWGVDLLKFDGCYCDSLENLADGYKHMSLALNRTGRSIVYSCEWPLYMWPFQKPNYTEIRQYCNHWRNFADIDDSWKSIKSILDWTSFNQERIVDVAGPGGWNDPDMLVIGNFGLSWNQQVTQMALWAIMAAPLFMSNDLRHISPQAKALLQDKDVIAINQDPLGKQGYQLRQGDNFEVWERPLSGLAWAVAMINRQEIGGPRSYTIAVASLGKGVACNPACFITQLLPVKRKLGFYEWTSRLRSHINPTGTVLLQLENTMQMSLKDLL
Host
Rabbit
Reactivity
Human
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Cell lysate)
GLA MaxPab rabbit polyclonal antibody. Western Blot analysis of GLA expression in HeLa.Western Blot (Transfected lysate)
Western Blot analysis of GLA expression in transfected 293T cell line (H00002717-T02) by GLA MaxPab polyclonal antibody.
Lane 1: GLA transfected lysate(48.80 KDa).
Lane 2: Non-transfected lysate.
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Gene Info — GLA
Entrez GeneID
2717GeneBank Accession#
NM_000169.1Protein Accession#
NP_000160.1Gene Name
GLA
Gene Alias
GALA
Gene Description
galactosidase, alpha
Gene Ontology
HyperlinkGene Summary
This gene encodes 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. [provided by RefSeq
Other Designations
OTTHUMP00000023679|agalsidase alfa|alpha-D-galactosidase A|alpha-D-galactoside galactohydrolase 1|alpha-gal A|alpha-galactosidase A|melibiase
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Interactome
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Pathway
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Disease
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