NAT2 (NM_000015) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC209360L2V
- LentiORF®
Lenti ORF particles, NAT2 (mGFP-tagged) - Human N-acetyltransferase 2 (arylamine N-acetyltransferase) (NAT2), 200ul, >10^7 TU/mL
Lentiviral Particles: DDK DDK w/ Puro mGFP w/ Puro
AAV Particle: DDK
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USD 365.00
Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | NAT2 |
Synonyms | AAC2; NAT-2; PNAT |
Mammalian Cell Selection | None |
Vector | pLenti-C-mGFP |
ACCN | NM_000015 |
ORF Size | 870 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC209360).
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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_000015.2 |
RefSeq Size | 1317 bp |
RefSeq ORF | 873 bp |
Locus ID | 10 |
UniProt ID | P11245 |
Cytogenetics | 8p22 |
Domains | Acetyltransf2 |
Protein Families | Transmembrane |
Protein Pathways | Caffeine metabolism, Drug metabolism - other enzymes, Metabolic pathways |
MW | 33.5 kDa |
Gene Summary | This gene encodes an enzyme that functions to both activate and deactivate arylamine and hydrazine drugs and carcinogens. Polymorphisms in this gene are responsible for the N-acetylation polymorphism in which human populations segregate into rapid, intermediate, and slow acetylator phenotypes. Polymorphisms in this gene are also associated with higher incidences of cancer and drug toxicity. A second polymorphic arylamine N-acetyltransferase gene (NAT1), is located near this gene (NAT2). [provided by RefSeq, Sep 2019] |
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