PINK1 (NM_032409) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC206970L1V

  • LentiORF®

Lenti ORF particles, PINK1 (Myc-DDK tagged) - Human PTEN induced putative kinase 1 (PINK1), nuclear gene encoding mitochondrial protein, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

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


Buy this product and get 50% off on the Lenti RapidTiter kit. Use Code: Rapid50

USD 1,361.00

2 Weeks*

Size
    • 200 ul

Product Images

Frequently bought together (3)
Lenti ORF control particles of pLenti-C-Myc-DDK, >10^7 TU/mL, 0.5 mL
    • 500 ul

USD 365.00


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

USD 671.00


PINK1 Rabbit polyclonal Antibody
    • 100 ul

USD 365.00

Other products for "PINK1"

Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Symbol PINK1
Synonyms BRPK; PARK6
Mammalian Cell Selection None
Vector pLenti-C-Myc-DDK
ACCN NM_032409
ORF Size 1743 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC206970).
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_032409.1
RefSeq Size 2680 bp
RefSeq ORF 1746 bp
Locus ID 65018
UniProt ID Q9BXM7
Cytogenetics 1p36.12
Domains pkinase, TyrKc, S_TKc
Protein Families Druggable Genome, Protein Kinase
Protein Pathways Parkinson's disease
MW 62.7 kDa
Gene Summary This gene encodes a serine/threonine protein kinase that localizes to mitochondria. It is thought to protect cells from stress-induced mitochondrial dysfunction. Mutations in this gene cause one form of autosomal recessive early-onset Parkinson disease. [provided by RefSeq, Jul 2008]

{0} Product Review(s)

0 Product Review(s) Submit review

Be the first one to submit a review

Product Citations

*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.