C1orf21 Protein, chromosome 1 open reading frame 21

C1orf21

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C1orf21

Official Full Name chromosome 1 open reading frame 21
Synonyms C1ORF21;chromosome 1 open reading frame 21;15494;ENSG00000116667;PIG13;1q25;uncharacterized protein C1orf21;uncharacterized protein C1orf21;proliferation-inducing protein 13;cell proliferation-inducing gene 13 protein;
    • Species :
    • Human
    • Source :
    • HEK293
    • Tag :
    • N/A
    Species Cat.# Product name Source (Host) Tag Protein Length Price
    Human C1orf21-8167HCL Recombinant Human C1orf21 293 Cell Lysate HEK293 N/A

    C1orf21 involved in several pathways and played different roles in them. We selected most pathways C1orf21 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with C1orf21 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

    Pathway Name Pathway Related Protein

    C1orf21 has several biochemical functions, for example, protein binding. Some of the functions are cooperated with other proteins, some of the functions could acted by C1orf21 itself. We selected most functions C1orf21 had, and list some proteins which have the same functions with C1orf21. You can find most of the proteins on our site.

    Function Related Protein
    protein binding SMARCC2; STX8; MED10; KIF6; HADHA; TIMP2; DNAIC2; HSPB1; LENG1; JAGN1

    C1orf21 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 C1orf21 here. Most of them are supplied by our site. Hope this information will be useful for your research of C1orf21.

    DRAM1

    Fennell, DA; Myrand, SP; et al. Association between Gene Expression Profiles and Clinical Outcome of Pemetrexed-Based Treatment in Patients with Advanced Non-Squamous Non-Small Cell Lung Cancer: Exploratory Results from a Phase II Study. PLOS ONE 9:-(2014).
    Abdalla, EM; Mostowska, A; et al. A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family. ARCHIVES OF ORAL BIOLOGY 59:722-728(2014).

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