IL12RB1 (NM_153701) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC216444L3V
- LentiORF®
-
Lenti ORF particles, IL12RB1 (Myc-DDK tagged) - Human interleukin 12 receptor, beta 1 (IL12RB1), transcript variant 2, 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Product Name | IL12RB1 (NM_153701) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | CD212; IL-12R-BETA1; IL12RB; IMD30 |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_153701 |
ORF Size | 1143 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC216444).
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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_153701.1 |
RefSeq Size | 1881 bp |
RefSeq ORF | 1146 bp |
Locus ID | 3594 |
Protein Families | Druggable Genome, Transmembrane |
Protein Pathways | Cytokine-cytokine receptor interaction, Jak-STAT signaling pathway |
MW | 39.6 kDa |
Gene Summary | The protein encoded by this gene is a type I transmembrane protein that belongs to the hemopoietin receptor superfamily. This protein binds to interleukine 12 (IL12) with a low affinity, and is thought to be a part of IL12 receptor complex. This protein forms a disulfide-linked oligomer, which is required for its IL12 binding activity. The coexpression of this and IL12RB2 proteins was shown to lead to the formation of high-affinity IL12 binding sites and reconstitution of IL12 dependent signaling. Mutations in this gene impair the development of interleukin-17-producing T lymphocytes and result in increased susceptibility to mycobacterial and Salmonella infections. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014] |
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