GGT1 (NM_005265) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC223586L1V

  • LentiORF®

Lenti ORF particles, GGT1 (Myc-DDK tagged) - Human gamma-glutamyltransferase 1 (GGT1), transcript variant 1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

Lentiviral Particles: DDK DDK w/ Puro mGFP mGFP w/ Puro


Special Offer: Buy this product and get 50% off Lenti Control Particles. Learn More.

USD 1,080.00

2 Weeks*

Size
    • 200 ul

Product Images

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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Symbol GGT1
Synonyms CD224; D22S672; D22S732; GGT; GGT 1; GTG
Mammalian Cell Selection None
Vector pLenti-C-Myc-DDK
ACCN NM_005265
ORF Size 1707 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC223586).
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_005265.2
RefSeq Size 2431 bp
RefSeq ORF 1709 bp
Locus ID 2678
Cytogenetics 22q11.23
Domains G_glu_transpept
Protein Families Protease, Transmembrane
Protein Pathways Arachidonic acid metabolism, Cyanoamino acid metabolism, Glutathione metabolism, Metabolic pathways, Selenoamino acid metabolism, Taurine and hypotaurine metabolism
MW 61.2 kDa
Gene Summary The enzyme encoded by this gene is a type I gamma-glutamyltransferase that catalyzes the transfer of the glutamyl moiety of glutathione to a variety of amino acids and dipeptide acceptors. The enzyme is composed of a heavy chain and a light chain, which are derived from a single precursor protein. It is expressed in tissues involved in absorption and secretion and may contribute to the etiology of diabetes and other metabolic disorders. Multiple alternatively spliced variants have been identified. There are a number of related genes present on chromosomes 20 and 22, and putative pseudogenes for this gene on chromosomes 2, 13, and 22. [provided by RefSeq, Jan 2014]

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