anti-WASH Complex Subunit 5 (WASHC5) Anticorps

WASHC5 encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. De plus, nous expédions et WASH Complex Subunit 5 Kits (1) et beaucoup plus de produits pour cette protéine.

afficher tous les anticorps Gène GeneID UniProt
WASHC5 9897 Q12768
WASHC5 223593 Q8C2E7
WASHC5    
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Top anti-WASH Complex Subunit 5 Anticorps sur anticorps-enligne.fr

Showing 9 out of 11 products:

Catalogue No. Reactivité Hôte Conjugué Application Images Quantité Livraison Prix Détails
Humain Lapin Inconjugué IHC, IHC (p), WB 100 μL 11 to 14 Days
$537.17
Détails
Humain Lapin Inconjugué ELISA, WB Western blot analysis of KIAA0196 in human ovary tissue with KIAA0196 polyclonal antibody  at 1 ug/mL. 100 μg 11 to 12 Days
$356.00
Détails
Humain Lapin Inconjugué ELISA, WB Western blot analysis of Strumpellin in human ovary tissue lysate with Strumpellin antibody at 1 µg/mL. 0.1 mg 2 to 3 Days
$360.00
Détails
Humain Lapin Inconjugué WB   0.1 mg 11 to 14 Days
$551.83
Détails
Humain Lapin Inconjugué ELISA, WB   100 μg 1 to 2 Days
$394.90
Détails
Souris Lapin Inconjugué IHC, ELISA, WB   100 μL 11 to 14 Days
$551.83
Détails
Humain Lapin Inconjugué EIA, WB   0.1 mg 4 to 8 Days
$522.50
Détails
Souris Lapin Inconjugué EIA, IHC (fro), WB   0.2 mL 6 to 8 Days
$500.50
Détails
Humain Lapin Inconjugué EIA   50 μg 2 to 3 Days
$515.90
Détails

Plus d’anticorps contre WASH Complex Subunit 5 partenaires d’interaction

Human WASH Complex Subunit 5 (WASHC5) interaction partners

  1. clinical phenotype of the c.1771T>C mutation of KIAA0196 has a considerable heterogeneity and this mutation may be a common pathogenic site of KIAA0196 mutations among Chinese patients with hereditary spastic paraplegia

  2. A novel missense mutation was identified in the KIAA0196 gene in a Japanese patient with SPG8.

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

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

  5. 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.

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

  7. 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.

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

  9. 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.

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

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

  12. 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.

Mouse (Murine) WASH Complex Subunit 5 (WASHC5) interaction partners

  1. These results underscore a key role for the WASH complex and its core subunit, Str, in the endolysosomal system.

WASH Complex Subunit 5 (WASHC5) profil antigène

Profil protéine

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 WASHC5

  • WASH complex subunit 5 (WASHC5) anticorps
  • WASH complex subunit 5 (washc5) anticorps
  • WASH complex subunit 5 (Washc5) anticorps
  • AL022848 anticorps
  • C76463 anticorps
  • Kiaa0196 anticorps
  • mKIAA0196 anticorps
  • SPG8 anticorps
  • strumpellin anticorps

Protein level used designations for WASHC5

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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