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Invitrogen™ KIAA0196 Polyclonal Antibody

Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA530337
Description
Recommended positive controls: HeLa. Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
This gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease; a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive, lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts. More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases.
Specifications
| KIAA0196 | |
| Polyclonal | |
| Unconjugated | |
| WASHC5 | |
| AL022848; C76463; E430025E21Rik; KIAA0196; mKIAA0196; RGD1564420; RIKEN cDNA E430025E21 gene; RTSC; RTSC1; similar to Hypothetical protein MGC31278; SPG8; Strumpellin; uncharacterized protein LOC362919; WASH complex subunit 5; WASH complex subunit strumpellin; WASHC5 | |
| Rabbit | |
| Antigen affinity chromatography | |
| RUO | |
| 9897 | |
| Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
| Liquid |
| Immunohistochemistry (Paraffin), Western Blot | |
| 1 mg/mL | |
| PBS with 1% BSA, 20% glycerol and 0.01% thimerosal; pH 7 | |
| Q12768 | |
| WASHC5 | |
| Recombinant protein encompassing a sequence within the C-terminus region of human Strumpellin. The exact sequence is proprietary. | |
| 100 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
Safety and Handling
WARNING: Cancer - www.P65Warnings.ca.gov
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