C22ORF13 Protein, chromosome 22 open reading frame 13

C22ORF13

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C22ORF13

Official Full Name chromosome 22 open reading frame 13
Synonyms C22ORF13; chromosome 22 open reading frame 13; uncharacterized protein C22orf13; MGC1842; CG13760 gene product [Drosophila melanogaster] homolog; LLN4
    • Species :
    • Human
    • Source :
    • HEK293
    • Tag :
    • N/A
    Species Cat.# Product name Source (Host) Tag Protein Length Price
    Human C22orf13-8094HCL Recombinant Human C22orf13 293 Cell Lysate HEK293 N/A

    C22ORF13 involved in several pathways and played different roles in them. We selected most pathways C22ORF13 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with C22ORF13 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

    Pathway Name Pathway Related Protein

    C22ORF13 has several biochemical functions, for example, protein binding. Some of the functions are cooperated with other proteins, some of the functions could acted by C22ORF13 itself. We selected most functions C22ORF13 had, and list some proteins which have the same functions with C22ORF13. You can find most of the proteins on our site.

    Function Related Protein
    protein binding IMP4; ACAA1; DDX21; SEC22B; TCOF1; PEX10; PAGE1; THAP3; THOP1; MSTN

    C22ORF13 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 C22ORF13 here. Most of them are supplied by our site. Hope this information will be useful for your research of C22ORF13.

    CRX; TCF4; CTH; KRTAP10-7; KRT40; NGLY1; MME

    Krasileva, KV; Buffalo, V; et al. Separating homeologs by phasing in the tetraploid wheat transcriptome. GENOME BIOLOGY 14:-(2013).
    Hoppman-Chaney, N; Jang, JS; et al. In-frame Multi-Exon Deletion of SMC1A in a Severely Affected Female with Cornelia de Lange Syndrome. AMERICAN JOURNAL OF MEDICAL GENETICS PART A 158A:193-198(2012).

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