PARK7 (NM_001123377) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC225206L4V

  • LentiORF®

Lenti ORF particles, PARK7 (mGFP-tagged) - Human Parkinson disease (autosomal recessive, early onset) 7 (PARK7), transcript variant 2, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



Need custom lentivirus service?
Get a free quote

CNY 8,360.00


货期*
详询

规格
    • 200 ul

Product images

经常一起买 (3)
Lenti ORF control particles of pLenti-C-mGFP-P2A-Puro, >1x10^7 TU/ml, 0.5 ml
    • 500 ul

CNY 2,950.00


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

CNY 5,230.00


Rabbit monoclonal anti-PARK7 antibody for SISCAPA, clone OTIR4F10
    • 100 ul

CNY 4,066.00

Specifications

Product Data
Product Name PARK7 (NM_001123377) Human Tagged ORF Clone Lentiviral Particle
Synonyms DJ-1; DJ1; GATD2; HEL-S-67p
Vector pLenti-C-mGFP-P2A-Puro
ACCN NM_001123377
ORF Size 567 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC225206).
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_001123377.1, NP_001116849.1
RefSeq Size 921 bp
RefSeq ORF 570 bp
Locus ID 11315
Protein Families Druggable Genome, Protease
Protein Pathways Parkinson's disease
MW 19.9 kDa
Gene Summary The product of this gene belongs to the peptidase C56 family of proteins. It acts as a positive regulator of androgen receptor-dependent transcription. It may also function as a redox-sensitive chaperone, as a sensor for oxidative stress, and it apparently protects neurons against oxidative stress and cell death. Defects in this gene are the cause of autosomal recessive early-onset Parkinson disease 7. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]
*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.
Customer Reviews 
Loading...