GBA (NM_001005742) Human Mass Spec Standard

CAT#: PH312242

GBA MS Standard C13 and N15-labeled recombinant protein (NP_001005742)



  View other "GBA" proteins (16)

Need it in bulk or customized?
Get a free quote

CNY 14,250.00


货期*
5周

规格
    • 10 ug

Product images

经常一起买 (2)
GBA mouse monoclonal antibody, clone OTI4G4 (formerly 4G4)
    • 100 ul

CNY 1,999.00
CNY 2,700.00


Transient overexpression lysate of glucosidase, beta, acid (GBA), transcript variant 1
    • 100 ug

CNY 3,080.00

Specifications

Product Data
Description GBA MS Standard C13 and N15-labeled recombinant protein (NP_001005742)
Species Human
Expression Host HEK293
Expression cDNA Clone or AA Sequence RC212242
Predicted MW 59.72 kDa
Protein Sequence
Tag C-Myc/DDK
Purity > 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration >0.05 µg/µL as determined by microplate BCA method
Labeling Method Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine
Buffer 25 mM Tris-HCl, 100 mM glycine, pH 7.3
Reference Data
RefSeq NP_001005742
RefSeq Size 2413
RefSeq ORF 1608
Synonyms GBA1; GCB; GLUC
Locus ID 2629
Cytogenetics 1q22
Summary 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. [provided by RefSeq, Jan 2010]
Protein Families Druggable Genome
Protein Pathways Lysosome, Metabolic pathways, Other glycan degradation, Sphingolipid metabolism
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

Documents

Other Versions

Customer Reviews 
Loading...