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anti-KIAA0196 (KIAA0196) Antibodies

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 and KIAA0196 Kits (1) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
KIAA0196 9897 Q12768
KIAA0196 223593 Q8C2E7
KIAA0196    
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Top anti-KIAA0196 Antibodies at antibodies-online.com

Showing 10 out of 10 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated EIA, WB Western blot analysis of Strumpellin in human ovary tissue lysate with Strumpellin Antibody  at 1 μg/ml. 0.1 mg Log in to see 6 to 8 Days
$401.50
Details
Human Rabbit Un-conjugated IHC (p), WB 100 μL Log in to see 8 to 10 Days
$507.83
Details
Human Rabbit Un-conjugated ELISA, WB Western blot analysis of Strumpellin in human ovary tissue lysate with Strumpellin antibody at 1 µg/mL. 0.1 mg Log in to see 2 to 3 Days
$330.00
Details
Mouse Rabbit Un-conjugated IHC, ELISA, WB   100 μL Log in to see 8 to 10 Days
$551.83
Details
Human Rabbit Un-conjugated ELISA, WB   100 μL Log in to see 2 to 3 Days
$429.00
Details
Human Rabbit Un-conjugated WB   100 μg Log in to see 8 to 10 Days
$522.50
Details
Mouse Rabbit Un-conjugated EIA, IHC (fro), WB   0.2 mL Log in to see 6 to 8 Days
$533.50
Details
Human Rabbit Un-conjugated IHC, IHC (p), WB   0.1 mL Log in to see 6 to 9 Days
$452.81
Details
Mouse Rabbit Un-conjugated IHC, ELISA, WB   100 μL Log in to see 5 to 6 Days
$320.60
Details
Human Rabbit Un-conjugated EIA   50 μg Log in to see 9 to 11 Days
$375.38
Details

KIAA0196 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality
Human ,


Mouse (Murine)


Rat (Rattus)


Top referenced anti-KIAA0196 Antibodies

  1. Human Polyclonal KIAA0196 Primary Antibody for 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)

More Antibodies against 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 (show FKBP15 Antibodies) may play an important role in endocytosis and subsequent membrane trafficking by interacting with AP2 (show GTF3A Antibodies) through KIAA0196 and KIAA1033 (show KIAA1033 Antibodies)

  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

Protein 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 anti-KIAA0196 (KIAA0196) Antibodies

  • 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 anti-KIAA0196 (KIAA0196) Antibodies

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
Selected quality suppliers for anti-KIAA0196 (KIAA0196) Antibodies
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