GBA antibody [C1C3]

Eine Lieferung in diese Region ist nicht möglich.

SKU:: GTX101267
Zusätzliche Namen:: glucosylceramidase beta , GBA1 , GCB , GLUC
Anwendung:: WB, IHC-P, IF, ICC
Konzentration:: 1.25 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, 20% Glycerol, 0.025% ProClin 300.
Immunogen:: Recombinant protein encompassing a sequence within the C-terminus region of human GBA. The exact sequence is proprietary.
Klon:: C1C3
Uniprot:: P04062
Synonyme:: acid beta-glucosidase;alglucerase;beta-GC;beta-glucocerebrosidase;cholesterol glucosyltransferase;cholesteryl-beta-glucosidase;D-glucosyl-N-acylsphingosine glucohydrolase;GBA1;GCB;GLUC;glucocerebrosidase;glucosidase, beta, acid;glucosylceramidase-like protein;imiglucerase;lysosomal acid GCase;lysosomal acid glucosylceramidase;lysosomal glucocerebrosidase;SGTase
Weitere Details:: This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq]

Versandbedingungen:: Blue Ice