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Official Full Name chromosome 5 open reading frame 22
Synonyms C5ORF22;chromosome 5 open reading frame 22;25639;ENSG00000082213;5p13.3;FLJ11193, FLJ23805, MGC33010, DKFZp667N066;UPF0489 protein C5orf22;UPF0489 protein C5orf22;
    • Species :
    • Human
    • Source :
    • HEK293
    • HEK293T
    • Wheat Germ
    • Tag :
    • GST
    • Myc/DDK
    • N/A
    Species Cat.# Product name Source (Host) Tag Protein Length Price
    Human C5orf22-0083H Recombinant Human C5orf22 Protein, GST-Tagged Wheat Germ GST
    Human C5orf22-2425H Recombinant Human C5orf22 Protein, Myc/DDK-tagged, C13 and N15-labeled HEK293T Myc/DDK
    Human C5orf22-8018HCL Recombinant Human C5orf22 293 Cell Lysate HEK293 N/A

    c5orf22 involved in several pathways and played different roles in them. We selected most pathways c5orf22 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with c5orf22 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

    Pathway Name Pathway Related Protein

    c5orf22 has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by c5orf22 itself. We selected most functions c5orf22 had, and list some proteins which have the same functions with c5orf22. You can find most of the proteins on our site.

    Function Related Protein

    c5orf22 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 c5orf22 here. Most of them are supplied by our site. Hope this information will be useful for your research of c5orf22.

    ELOF1; WBP11

    Aschebrook-Kilfoy, B; Argos, M; et al. Genome-Wide Association Study of Parity in Bangladeshi Women. PLOS ONE 10:-(2015).
    Ajroud-Driss, S; Fecto, F; et al. Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy. NEUROGENETICS 16:1-9(2015).

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