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Official Full Name transmembrane 9 superfamily member 2
Synonyms TM9SF2;transmembrane 9 superfamily member 2;P76;76 kDa membrane protein;transmembrane protein 9 superfamily member 2;FLJ26287;MGC117391;
    • Species :
    • Mouse
    • Rat
    • Zebrafish
    • Source :
    • Mammalian Cell
    • Tag :
    • His
    Species Cat.# Product name Source (Host) Tag Protein Length Price
    Mouse TM9SF2-16847M Recombinant Mouse TM9SF2 Protein Mammalian Cell His
    Rat TM9SF2-6090R Recombinant Rat TM9SF2 Protein Mammalian Cell His
    Zebrafish TM9SF2-12000Z Recombinant Zebrafish TM9SF2 Mammalian Cell His

    tm9sf2 involved in several pathways and played different roles in them. We selected most pathways tm9sf2 participated on our site, such as content, which may be useful for your reference. Also, other proteins which involved in the same pathway with tm9sf2 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

    Pathway Name Pathway Related Protein

    tm9sf2 has several biochemical functions, for example, Content. Some of the functions are cooperated with other proteins, some of the functions could acted by tm9sf2 itself. We selected most functions tm9sf2 had, and list some proteins which have the same functions with tm9sf2. You can find most of the proteins on our site.

    Function Related Protein
    molecular_function ARGLU1A; MS4A6B; NRN1B; CHCHD6A; VGLL4L; TRAM1L1; GM10486; SMIM15; GM8660; TMEM57

    tm9sf2 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 tm9sf2 here. Most of them are supplied by our site. Hope this information will be useful for your research of tm9sf2.

    Chinen, J; Martinez-Gallo, M; et al. Transmembrane activator and CAML interactor (TACI) haploinsufficiency results in B-cell dysfunction in patients with Smith-Magenis syndrome. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY 127:1579-1586(2011).
    Salzer, U; Bacchelli, C; et al. Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes. BLOOD 113:1967-1976(2009).

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