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RAET1G

  • Official Full Name

    retinoic acid early transcript 1G

Species Cat.# Product name Source (Host) Tag Protein Length Price
Human RAET1G-629H Active Recombinant Human RAET1G, His-tagged CHO His
Human RAET1G-1462HCL Recombinant Human RAET1G cell lysate N/A
  • Involved Pathway
  • Protein Function
  • Interacting Protein
  • RAET1G Related Articles
  • RAET1G Related Research Area

RAET1G involved in several pathways and played different roles in them. We selected most pathways RAET1G participated on our site, such as Natural killer cell mediated cytotoxicity, which may be useful for your reference. Also, other proteins which involved in the same pathway with RAET1G were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

Pathway Name Pathway Related Protein
Natural killer cell mediated cytotoxicityIFNA7;PIK3R2;Fasl;ARAF;HLA-C;LCK;KLRC4-KLRK1;FCER1G;IFNA2

RAET1G has several biochemical functions, for example, natural killer cell lectin-like receptor binding. Some of the functions are cooperated with other proteins, some of the functions could acted by RAET1G itself. We selected most functions RAET1G had, and list some proteins which have the same functions with RAET1G. You can find most of the proteins on our site.

Function Related Protein
natural killer cell lectin-like receptor bindingH60a;ULBP1;HLA-E;RAET1E;RAET1L;ULBP3;ULBP2;RAET1G;Mill2

RAET1G has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with RAET1G here. Most of them are supplied by our site. Hope this information will be useful for your research of RAET1G.

KLRK1

Cho, H; Chung, JY; et al. MICA/B and ULBP1 NKG2D ligands are independent predictors of good prognosis in cervical cancer. BMC CANCER 14:-(2014).
Rareongjai, S; Romphruk, A; et al. Linkage disequilibrium of polymorphic RAET1 genes in Thais. TISSUE ANTIGENS 76:230-235(2010).
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