Growth hormone receptor (GHR) (NM_000163) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC218710L3V
- LentiORF®
Lenti ORF particles, GHR (Myc-DDK-tagged)-Human growth hormone receptor (GHR), 200ul, >10^7 TU/mL
Buy this product and get 50% off on the Lenti RapidTiter kit. Use Code: Rapid50
Frequently bought together (3)
Lenti ORF control particles of pLenti-C-Myc-DDK-P2A-Puro, >1x10^7 TU/ml, 0.5 ml
USD 310.00
Other products for "GHR"
Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | Myc-DDK |
Symbol | GHR |
Synonyms | GHBP; GHIP |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_000163 |
ORF Size | 1914 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC218710).
|
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_000163.2 |
RefSeq Size | 4370 bp |
RefSeq ORF | 1917 bp |
Locus ID | 2690 |
UniProt ID | P10912 |
Cytogenetics | 5p13.1-p12 |
Protein Families | Druggable Genome, Transmembrane |
Protein Pathways | Cytokine-cytokine receptor interaction, Jak-STAT signaling pathway, Neuroactive ligand-receptor interaction |
MW | 71.5 kDa |
Gene Summary | This gene encodes a member of the type I cytokine receptor family, which is a transmembrane receptor for growth hormone. Binding of growth hormone to the receptor leads to receptor dimerization and the activation of an intra- and intercellular signal transduction pathway leading to growth. Mutations in this gene have been associated with Laron syndrome, also known as the growth hormone insensitivity syndrome (GHIS), a disorder characterized by short stature. In humans and rabbits, but not rodents, growth hormone binding protein (GHBP) is generated by proteolytic cleavage of the extracellular ligand-binding domain from the mature growth hormone receptor protein. Multiple alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Jun 2011] |
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