SMPD1 Rabbit mAb - A23894
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Catalog #
AB-A23894
Ab
135,00 €
The protein encoded by this gene is a lysosomal acid sphingomyelinase that converts sphingomyelin to ceramide. The encoded protein also has phospholipase C activity. Defects in this gene are a cause of Niemann-Pick disease type A (NPA) and Niemann-Pick disease type B (NPB). Multiple transcript variants encoding different isoforms have been identified.
| Isotype | IgG |
|---|---|
| Datasheet URL | https://abclonal.com/instructions/pdf/A23894 |
| Alternative Names | ASM; NPD; ASMASE; D1 |
| Species | Human |
| Source | Rabbit |
| Purity | Affinity purification |
| Immunogen | Recombinant fusion protein containing a sequence corresponding to amino acids 70-340 of human SMPD1(NP_000534.3). |
| Storage | Store at -20℃. Avoid freeze / thaw cycles.|Buffer: PBS with 0.05% proclin300,0.05% BSA,50% glycerol,pH7.3. |
| Conjugate | Unconjugated |