GNB3 (NM_002075) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC200470L4V

  • LentiORF®

Lenti ORF particles, GNB3 (mGFP-tagged) - Human guanine nucleotide binding protein (G protein), beta polypeptide 3 (GNB3), 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



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CNY 9,975.00


货期*
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规格
    • 200 ul

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Specifications

Product Data
Product Name GNB3 (NM_002075) Human Tagged ORF Clone Lentiviral Particle
Synonyms CSNB1H
Vector pLenti-C-mGFP-P2A-Puro
ACCN NM_002075
ORF Size 1020 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC200470).
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_002075.2
RefSeq Size 1760 bp
RefSeq ORF 1023 bp
Locus ID 2784
Protein Families Druggable Genome
Protein Pathways Chemokine signaling pathway, Taste transduction
MW 37.3 kDa
Gene Summary Heterotrimeric guanine nucleotide-binding proteins (G proteins), which integrate signals between receptors and effector proteins, are composed of an alpha, a beta, and a gamma subunit. These subunits are encoded by families of related genes. This gene encodes a beta subunit which belongs to the WD repeat G protein beta family. Beta subunits are important regulators of alpha subunits, as well as of certain signal transduction receptors and effectors. A single-nucleotide polymorphism (C825T) in this gene is associated with essential hypertension and obesity. This polymorphism is also associated with the occurrence of the splice variant GNB3-s, which appears to have increased activity. GNB3-s is an example of alternative splicing caused by a nucleotide change outside of the splice donor and acceptor sites. Alternative splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Jul 2014]
*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.
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