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  2. Polyclonal

GTX115311

Strumpellin antibody [C2C3], C-term

Eine Lieferung in diese Region ist nicht möglich.

SKU:
GTX115311
Zusätzliche Namen:
WASH complex subunit 5 , KIAA0196 , RTSC , RTSC1 , SPG8
Anwendung:
WB, IHC-P
Konzentration:
1 mg/ml
Physischer Zustand:
Liquid
Spezies-Reaktivität:
Human
Aufreinigung:
Affinity Purified
Lagerbedingungen:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Hersteller:
Genetex
Host:
Rabbit
Reaktivitäten:
Human
Buffer:
PBS, 1% BSA, 20% Glycerol, 0.01% Thimerosal.
Immunogen:
Recombinant protein encompassing a sequence within the C-terminus region of human Strumpellin. The exact sequence is proprietary.
Klon:
C2C3
Uniprot:
Q12768
Synonyme:
KIAA0196;RTSC;RTSC1;SPG8;strumpellin;WASH complex subunit 5;WASH complex subunit strumpellin
Weitere Details:
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. [provided by RefSeq]
Versandbedingungen:
Blue Ice