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GM2A Polyclonal Antibody, Invitrogen™
Rabbit Polyclonal Antibody
Brand: Invitrogen PA525737
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Description
This antibody is predicted to react with non-human primate based on sequence homology.
This gene encodes a small glycolipid transport protein which acts as a substrate specific co-factor for the lysosomal enzyme beta-hexosaminidase A. Beta-hexosaminidase A, together with GM2 ganglioside activator, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene result in GM2-gangliosidosis type AB or the AB variant of Tay-Sachs disease. Alternative splicing results in multiple transcript variants.
Specifications
| GM2A | |
| Polyclonal | |
| PBS with 0.09% sodium azide | |
| P17900, Q60648 | |
| GM2A | |
| KLH conjugated synthetic peptide between 25-54 amino acids from the N-terminal region of human GM2A | |
| 400 μL | |
| Primary | |
| Human, Mouse | |
| Antibody | |
| IgG |
| Western Blot | |
| Unconjugated | |
| GM2A | |
| AA408702; AW215435; cerebroside sulfate activator protein; Ganglioside GM2 activator; Ganglioside GM2 activator isoform short; GM2 ganglioside activator; GM2 ganglioside activator protein; Gm2a; GM2-AP; SAP-3; shingolipid activator protein 3; sphingolipid activator protein 3 | |
| Rabbit | |
| Antigen affinity chromatography, Protein A | |
| RUO | |
| 14667, 2760 | |
| -20° C, Avoid Freeze/Thaw Cycles | |
| Liquid |
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