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Official Full Name chromosome 11 open reading frame 46
Synonyms C11ORF46; chromosome 11 open reading frame 46; uncharacterized protein C11orf46; FLJ38968; DJ299F11.1; Hypothetical protein LOC120534
    • Species :
    • Human
    • Source :
    • HEK293
    • Wheat Germ
    • Tag :
    • GST
    • N/A
    Species Cat.# Product name Source (Host) Tag Protein Length Price
    Human C11orf46-468H Recombinant Human C11orf46 Protein, GST-tagged Wheat Germ GST
    Human C11orf46-8351HCL Recombinant Human C11orf46 293 Cell Lysate HEK293 N/A

    c11orf46 involved in several pathways and played different roles in them. We selected most pathways c11orf46 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with c11orf46 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

    Pathway Name Pathway Related Protein

    c11orf46 has several biochemical functions, for example, protein binding. Some of the functions are cooperated with other proteins, some of the functions could acted by c11orf46 itself. We selected most functions c11orf46 had, and list some proteins which have the same functions with c11orf46. You can find most of the proteins on our site.

    Function Related Protein
    protein binding RBMX; RC3H2; EFCAB11; RNF6; NITR9; FAM192A; GPR37; FAM122A; PAQR5; ZNF664-FAM101A

    c11orf46 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 c11orf46 here. Most of them are supplied by our site. Hope this information will be useful for your research of c11orf46.

    SETDB2; ARL14; MYO1E; lepB; ezrA; Setdb1

    Ramasamy, A; Curjuric, I; et al. A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY 128:996-1005(2011).
    Schneider, E; Marker, T; et al. Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment. HUMAN MOLECULAR GENETICS 18:655-666(2009).

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