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Home TrueClone GBA Clone

GBA (NM_000157) Human cDNA Clone

Specifications Citations Clones of Other Species Product Documents
SKU Description Price Availibility*  
SC120080 GBA (untagged)-Human glucosidase, beta, acid (GBA), transcript variant 1 (10ug), NM_000157.2, 10ug $185 In Stock
TF81001 TurboFectin, High performance Transfection reagent (1ml/vial) $420 In Stock
TA308240 Rabbit Polyclonal antibody to GBA (glucosidase, beta, acid), 100ul $325 In Stock
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Also for GBA (NM_000157)
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OriGene Data
Vector:pCMV6-XL5 Insert Size: 2290 Restriction Site: NotI-NotI
Sequence Data: Fully Sequenced ORF          5' Read Nucleotide Sequence          3' Read Nucleotide Sequence         
OTI Disclaimer: Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Product Components: The cDNA clone is shipped in a 2-D bar-coded Matrix tube as dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. Every lot of primer is tested to provide clean sequencing of OriGene TrueClones.
Protein Families: Druggable Genome
Protein Pathways: Other glycan degradationSphingolipid metabolismMetabolic pathwaysLysosome
Reference Data
RefSeq: NM_000157.2, NP_000148
RefSeq Size: 2324 RefSeq ORF: 1611
Synonyms : GBA1; GCB; GLUC
LocusID: 2629 Cytogenetic: 1q21 Domains: Glyco_hydro_30
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].

Transcript Variant: This variant (1) encodes isoform 1. Variants 1, 2 and 3 encode the same isoform 1.

* Delivery time is an estimate in business days. Occasional delays may occur due to unforeseen complexities in the preparation of your construct. International customers may expect an additional 1-2 weeks in shipping

 

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