Probable hydrolase PNKD (PNKD) (NM_015488) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC206179L3V

  • LentiORF®

Lenti ORF particles, PNKD (Myc-DDK tagged) - Human paroxysmal nonkinesigenic dyskinesia (PNKD), nuclear gene encoding mitochondrial protein, transcript variant 1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

Lentiviral Particles: DDK w/ Puro mGFP w/ Puro

AAV Particle: DDK


Biosafety Sheet

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

USD 1,007.00

7 Weeks*

Size
    • 200 ul

Product Images

Frequently bought together (3)
PNKD rabbit polyclonal antibody
    • 100 ul

USD 380.00


Lenti ORF control particles of pLenti-C-Myc-DDK-P2A-Puro, >1x10^7 TU/ml, 0.5 ml
    • 500 ul

USD 365.00


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

USD 671.00

Other products for "PNKD"

Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Symbol PNKD
Synonyms BRP17; DYT8; FKSG19; FPD1; KIPP1184; MR-1; MR-1S; MR1; PDC; PKND1; PNKD1; R1; TAHCCP2
Mammalian Cell Selection Puromycin
Vector pLenti-C-Myc-DDK-P2A-Puro
ACCN NM_015488
ORF Size 1155 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC206179).
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_015488.4
RefSeq Size 3129 bp
RefSeq ORF 1158 bp
Locus ID 25953
UniProt ID Q8N490
Cytogenetics 2q35
Protein Families Transmembrane
MW 42.9 kDa
Gene Summary This gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]

{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.