PYROXD1 (NM_024854) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC204614L3V

  • LentiORF®

Lenti ORF particles, PYROXD1 (Myc-DDK tagged) - Human pyridine nucleotide-disulphide oxidoreductase domain 1 (PYROXD1), 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



Need custom lentivirus service?
Get a free quote

CNY 8,930.00


货期*
详询

规格
    • 200 ul

Product images

经常一起买 (3)
Lenti ORF control particles of pLenti-C-Myc-DDK-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 Polyclonal Anti-PYROXD1 Antibody
    • 100 ul

CNY 5,250.00

Specifications

Product Data
Product Name PYROXD1 (NM_024854) Human Tagged ORF Clone Lentiviral Particle
Synonyms MFM8
Vector pLenti-C-Myc-DDK-P2A-Puro
ACCN NM_024854
ORF Size 1500 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC204614).
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_024854.2
RefSeq Size 4136 bp
RefSeq ORF 1503 bp
Locus ID 79912
Domains pyr_redox
Protein Families Druggable Genome
MW 55.8 kDa
Gene Summary This gene encodes a nuclear-cytoplasmic pyridine nucleotide-disulphide reductase (PNDR). PNDRs are flavoproteins that catalyze the pyridine nucleotide-dependent reduction of thiol residues in other proteins. The encoded protein belongs to the class I pyridine nucleotide-disulphide oxidoreductase family but lacks the C-terminal dimerization domain found in other family members and instead has a C-terminal nitrile reductase domain. It localizes to the nucleus and to striated sarcomeric compartments. Naturally occurring mutations in this gene cause early-onset myopathy with internalized nuclei and myofibrillar disorganization. A pseudogene of this gene has been defined on chromosome 11. [provided by RefSeq, Apr 2017]
*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...