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KIAA0196 (KIAA0196) ELISA Kits

KIAA0196 encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. Additionally we are shipping KIAA0196 Antibodies (10) and and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
KIAA0196 9897 Q12768
Anti-Mouse KIAA0196 KIAA0196 223593 Q8C2E7
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Top KIAA0196 ELISA Kits at antibodies-online.com

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Catalog No. Reactivity Sensitivity Range Quantity Supplier Delivery Price Details
Human 4.69 pg/ml 18.75-1200 pg/mL 96 Tests Log in to see 11 to 13 Days
$910.56
Details

More ELISA Kits for KIAA0196 Interaction Partners

Human KIAA0196 interaction partners

  1. A mutation in the WASH component KIAA0196 (strumpellin) is associated with hypercholesterolaemia in humans.

  2. Study found a novel KIAA0196 (SPG8) mutation in a Chinese family with spastic paraplegia.

  3. To identify the underlying genetic cause of Ritscher-Schinzel syndrome, affected individuals from a First Nations community in Manitoba underwent mutational analysis. All eight patients were homozygous for a novel splice site mutation in KIAA0196.

  4. we identified a novel KIAA0196 missense variant in the proband and her daughter expanding the clinical spectrum of hereditary spastic paraplegia 8.

  5. We have identified a fourth pathogenic KIAA0196 mutation in a Dutch hereditary spastic paraplegia family, the seventh family worldwide, with a less severe clinical course than described before.

  6. Strumpellin disease mutations do not affect its incorporation into the WASH complex or its subcellular localisation.

  7. strumpellin is a ubiquitously expressed protein present in cytosolic and endoplasmic reticulum cell fractions. In the human central nervous system strumpellin shows a presynaptic localization.

  8. WAFL may play an important role in endocytosis and subsequent membrane trafficking by interacting with AP2 through KIAA0196 and KIAA1033

  9. The expression of KIAA0196 at chromosomal region 8q24 is significantly higher in prostate carcinomas with gene amplification than in those without it.

  10. Identified three mutations in the KIAA0196 gene in six families that map to the SPG8 locus. The identification and characterization of the KIAA0196 gene will enable further insight into the pathogenesis of HSP.

KIAA0196 Antigen Profile

Antigen Summary

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.

Gene names and symbols associated with KIAA0196 (KIAA0196) ELISA Kits

  • KIAA0196 (KIAA0196) antibody
  • KIAA0196 (kiaa0196) antibody
  • RIKEN cDNA E430025E21 gene (E430025E21Rik) antibody
  • AL022848 antibody
  • C76463 antibody
  • Kiaa0196 antibody
  • mKIAA0196 antibody
  • SPG8 antibody
  • strumpellin antibody

Protein level used designations for KIAA0196 (KIAA0196) ELISA Kits

KIAA0196 , WASH complex subunit strumpellin , Strumpellin , strumpellin

GENE ID SPECIES
420334 Gallus gallus
448397 Xenopus (Silurana) tropicalis
464385 Pan troglodytes
9897 Homo sapiens
100173723 Pongo abelii
223593 Mus musculus
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