IGF2R (NM_000876) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC215594L1V

  • LentiORF®

Lenti ORF particles, IGF2R (Myc-DDK tagged) - Human insulin-like growth factor 2 receptor (IGF2R), 200ul, >10^7 TU/mL

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USD 2,399.00

In Stock*

Size
    • 200 ul

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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Symbol IGF2R
Synonyms CD222; CI-M6PR; CIMPR; M6P-R; M6P/IGF2R; MPR1; MPR 300; MPR300; MPRI
Vector pLenti-C-Myc-DDK
ACCN NM_000876
ORF Size 7473 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC215594).
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_000876.1, NP_000867.1
RefSeq Size 9090 bp
RefSeq ORF 7476 bp
Locus ID 3482
UniProt ID P11717
Cytogenetics 6q25.3
Protein Families Druggable Genome, Transmembrane
Protein Pathways Lysosome
MW 274.26 kDa
Gene Summary 'This gene encodes a receptor for both insulin-like growth factor 2 and mannose 6-phosphate. The binding sites for each ligand are located on different segments of the protein. This receptor has various functions, including in the intracellular trafficking of lysosomal enzymes, the activation of transforming growth factor beta, and the degradation of insulin-like growth factor 2. Mutation or loss of heterozygosity of this gene has been association with risk of hepatocellular carcinoma. The orthologous mouse gene is imprinted and shows exclusive expression from the maternal allele; however, imprinting of the human gene may be polymorphic, as only a minority of individuals showed biased expression from the maternal allele (PMID:8267611). [provided by RefSeq, Nov 2015]'

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