SHP2 (PTPN11) (NM_002834) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC220029L4V

  • LentiORF®

Lenti ORF particles, PTPN11 (mGFP-tagged)-Human protein tyrosine phosphatase, non-receptor type 11 (PTPN11), 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



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CNY 11,780.00


货期*
详询

规格
    • 200 ul

Product images

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Specifications

Product Data
Product Name SHP2 (PTPN11) (NM_002834) Human Tagged ORF Clone Lentiviral Particle
Synonyms BPTP3; CFC; JMML; METCDS; NS1; PTP-1D; PTP2C; SH-PTP2; SH-PTP3; SHP2
Vector pLenti-C-mGFP-P2A-Puro
ACCN NM_002834
ORF Size 1779 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC220029).
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_002834.3
RefSeq Size 6300 bp
RefSeq ORF 1782 bp
Locus ID 5781
Protein Families Druggable Genome, Phosphatase
Protein Pathways Adipocytokine signaling pathway, Chronic myeloid leukemia, Epithelial cell signaling in Helicobacter pylori infection, Jak-STAT signaling pathway, Leukocyte transendothelial migration, Natural killer cell mediated cytotoxicity, Neurotrophin signaling pathway, Renal cell carcinoma
MW 67.8 kDa
Gene Summary The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains two tandem Src homology-2 domains, which function as phospho-tyrosine binding domains and mediate the interaction of this PTP with its substrates. This PTP is widely expressed in most tissues and plays a regulatory role in various cell signaling events that are important for a diversity of cell functions, such as mitogenic activation, metabolic control, transcription regulation, and cell migration. Mutations in this gene are a cause of Noonan syndrome as well as acute myeloid leukemia. [provided by RefSeq, Aug 2016]
*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.
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