GBA (NM_000157) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC216061L2V

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  • LentiORF®

Lenti ORF particles, GBA (mGFP-tagged) - Human glucosidase, beta, acid (GBA), transcript variant 1, 200ul, >10^7 TU/mL



USD 1,049.00

3 Weeks*

Size
    • 200 ul

Product images

Frequently bought together (2)
Lenti ORF control particles of pLenti-C-mGFP, >10^7 TU/mL, 0.5 mL
    • 500 ul

USD 365.00


One-Wash Lentivirus Titer Kit, HIV-1 p24 ELISA
    • 96 reactions

USD 671.00

Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag mGFP
Symbol GBA
Synonyms GBA1; GCB; GLUC
Mammalian Cell Selection None
Vector pLenti-C-mGFP
ACCN NM_000157
ORF Size 1608 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC216061).
OTI Disclaimer The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
OTI Annotation This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.
Reference Data
RefSeq NM_000157.2
RefSeq Size 2324 bp
RefSeq ORF 1611 bp
Locus ID 2629
UniProt ID P04062
Cytogenetics 1q22
Domains Glyco_hydro_30
Protein Families Druggable Genome
Protein Pathways Lysosome, Metabolic pathways, Other glycan degradation, Sphingolipid metabolism
MW 59.72 kDa
Gene 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]
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*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.