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KIAA0196, Rabbit, Polyclonal Antibody, Abnova™
Rabbit polyclonal antibody raised against synthetic peptide of KIAA0196.
Supplier: Abnova Corporation PAB25762
Description
This gene encodes a 134kDa 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. [provided by RefSeq
Specifications
KIAA0196 | |
Polyclonal | |
Unconjugated | |
Western Blot (1 ug/mL) The optimal working dilution should be determined by the end user. | |
KIAA0196 | |
KIAA0196 | |
A synthetic peptide corresponding to 19 amino acids at C-terminus of human KIAA0196. | |
100 μg | |
Primary | |
Multiple isoforms of Strumpellin are known to exist. | |
Store at 4°C for three months. For long term storage store at -20°C. Aliquot to avoid repeated freezing and thawing. |
|
IgG |
ELISA, Western Blot | |
1 mg/mL | |
Rabbit polyclonal antibody raised against synthetic peptide of KIAA0196. | |
In PBS (0.02% sodium azide) | |
MGC111053/SPG8 | |
Rabbit | |
Peptide affinity purification | |
RUO | |
9897 | |
Human, Mouse, Rat | |
Liquid |
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