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anti-KIAA0196 (KIAA0196) Antikörper

KIAA0196 encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. Zusätzlich bieten wir Ihnen KIAA0196 Kits (1) und viele weitere Produktgruppen zu diesem Protein an.

Alle Antikörper anzeigen Gen GeneID UniProt
KIAA0196 9897 Q12768
KIAA0196 223593 Q8C2E7
KIAA0196    
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Top anti-KIAA0196 Antikörper auf antikoerper-online.de

Showing 10 out of 10 products:

Katalog Nr. Reaktivität Wirt Konjugat Applikation Bilder Menge Anbieter Lieferzeit Preis Details
Human Kaninchen Unkonjugiert EIA, WB Western blot analysis of Strumpellin in human ovary tissue lysate with Strumpellin Antibody  at 1 μg/ml. 0.1 mg Anmelden zum Anzeigen 8 bis 10 Tage
357,50 €
Details
Human Kaninchen Unkonjugiert IHC (p), WB 100 μL Anmelden zum Anzeigen 11 bis 14 Tage
600,64 €
Details
Human Kaninchen Unkonjugiert IHC (p), WB 0.1 mL Anmelden zum Anzeigen 6 bis 8 Tage
385,00 €
Details
Human Kaninchen Unkonjugiert WB Western blot analysis of Strumpellin in human ovary tissue lysate with Strumpellin antibody at 1 µg/mL. 0.1 mg Anmelden zum Anzeigen 6 bis 8 Tage
377,14 €
Details
Maus Kaninchen Unkonjugiert IHC, WB   100 μL Anmelden zum Anzeigen 11 bis 14 Tage
653,02 €
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Human Kaninchen Unkonjugiert WB   100 μL Anmelden zum Anzeigen 6 bis 8 Tage
434,76 €
Details
Maus Kaninchen Unkonjugiert IHC (fro), EIA, WB   0.2 mL Anmelden zum Anzeigen 8 bis 10 Tage
440,00 €
Details
Human Kaninchen Unkonjugiert WB   100 μg Anmelden zum Anzeigen 11 bis 14 Tage
618,10 €
Details
Maus Kaninchen Unkonjugiert WB, IHC   100 μL Anmelden zum Anzeigen 2 bis 3 Tage
266,40 €
Details
Human Kaninchen Unkonjugiert EIA   50 μg Anmelden zum Anzeigen 6 bis 8 Tage
396,00 €
Details

KIAA0196 Antikörper nach Reaktivität, Anwendung, Klonalität and Konjugat

Attribute Applikationen Wirt Klonalität
Human , , ,

Mouse (Murine) , , , ,

Rat (Rattus) , ,

Am meisten referenzierte anti-KIAA0196 Antikörper

  1. Human Polyclonal KIAA0196 Primary Antibody für EIA,WB - ABIN1450091 : Valdmanis, Meijer, Reynolds, Lei, MacLeod, Schlesinger, Zatz, Reid, Dion, Drapeau, Rouleau: Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia. in American journal of human genetics 2006 (PubMed)

Weitere Antikörper gegen KIAA0196 Interaktionspartner

Human KIAA0196 Interaktionspartner

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

  2. 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.

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

  4. 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.

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

  6. 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.

  7. WAFL (zeige FKBP15 Antikörper) may play an important role in endocytosis and subsequent membrane trafficking by interacting with AP2 (zeige GTF3A Antikörper) through KIAA0196 and KIAA1033 (zeige KIAA1033 Antikörper)

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

  9. 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-Profil

Protein Überblick

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.

Genbezeichner und Symbole assoziert mit anti-KIAA0196 (KIAA0196) Antikörper

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

Bezeichner auf Proteinebene für anti-KIAA0196 (KIAA0196) Antikörper

KIAA0196 , WASH complex subunit strumpellin , Strumpellin , strumpellin

GENE ID SPEZIES
420334 Gallus gallus
448397 Xenopus (Silurana) tropicalis
464385 Pan troglodytes
9897 Homo sapiens
100173723 Pongo abelii
223593 Mus musculus
Ausgewählte Anbieter für anti-KIAA0196 (KIAA0196) Antikörper
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