JAK3 (NM_000215) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC217928L1V

  • LentiORF®

Lenti ORF particles, JAK3 (Myc-DDK tagged) - Human Janus kinase 3 (JAK3), 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



Need custom lentivirus service?
Get a free quote

CNY 19,190.00


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, >10^7 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


JAK3 mouse monoclonal antibody,clone OTI1B4
    • 100 ul

CNY 1,999.00
CNY 2,700.00

Specifications

Product Data
Product Name JAK3 (NM_000215) Human Tagged ORF Clone Lentiviral Particle
Synonyms JAK-3; JAK3_HUMAN; JAKL; L-JAK; LJAK
Vector pLenti-C-Myc-DDK
ACCN NM_000215
ORF Size 3372 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC217928).
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_000215.2
RefSeq Size 4025 bp
RefSeq ORF 3375 bp
Locus ID 3718
Domains B41, pkinase, SH2, TyrKc, S_TKc
Protein Families Druggable Genome, Protein Kinase
Protein Pathways Chemokine signaling pathway, Jak-STAT signaling pathway, Primary immunodeficiency
MW 124.9 kDa
Gene Summary The protein encoded by this gene is a member of the Janus kinase (JAK) family of tyrosine kinases involved in cytokine receptor-mediated intracellular signal transduction. It is predominantly expressed in immune cells and transduces a signal in response to its activation via tyrosine phosphorylation by interleukin receptors. Mutations in this gene are associated with autosomal SCID (severe combined immunodeficiency disease). [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...