Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Strumpellin antibody (AA 380-530)

WASHC5 Reactivity: Human WB, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7271349
  • Target See all Strumpellin (WASHC5) Antibodies
    Strumpellin (WASHC5) (WASH Complex Subunit 5 (WASHC5))
    Binding Specificity
    • 3
    • 1
    • 1
    AA 380-530
    Reactivity
    • 4
    • 4
    • 2
    Human
    Host
    • 5
    Rabbit
    Clonality
    • 5
    Polyclonal
    Conjugate
    • 5
    This Strumpellin antibody is un-conjugated
    Application
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Purpose
    KIAA0196 Rabbit pAb
    Cross-Reactivity
    Mouse, Rat
    Characteristics
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein containing a sequence corresponding to amino acids 380-530 of human KIAA0196 (NP_055661.3).
    Isotype
    IgG
  • Application Notes
    WB,1:500 - 1:2000,IHC,1:50 - 1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Strumpellin (WASHC5) (WASH Complex Subunit 5 (WASHC5))
    Alternative Name
    KIAA0196 (WASHC5 Products)
    Synonyms
    SPG8 antibody, AL022848 antibody, C76463 antibody, Kiaa0196 antibody, mKIAA0196 antibody, strumpellin antibody, WASH complex subunit 5 antibody, WASHC5 antibody, washc5 antibody, Washc5 antibody
    Background
    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.,RTSC, SPG8, RTSC1, KIAA0196,KIAA0196
    Gene ID
    9897
    UniProt
    Q12768
You are here: