C14orf43 Protein, chromosome 14 open reading frame 43

C14orf43

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C14orf43

Official Full Name chromosome 14 open reading frame 43
Synonyms C14ORF43;chromosome 14 open reading frame 43;19853;ENSG00000156030;LSR68;c14_5541;C14orf117;14q24.3;FLJ00335;uncharacterized protein C14orf43;uncharacterized protein C14orf43;
    • Species :
    • Human
    • Source :
    • HEK293
    • Tag :
    • N/A
    Species Cat.# Product name Source (Host) Tag Protein Length Price
    Human C14orf43-8276HCL Recombinant Human C14orf43 293 Cell Lysate HEK293 N/A

    C14orf43 involved in several pathways and played different roles in them. We selected most pathways C14orf43 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with C14orf43 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

    Pathway Name Pathway Related Protein

    C14orf43 has several biochemical functions, for example, DNA binding. Some of the functions are cooperated with other proteins, some of the functions could acted by C14orf43 itself. We selected most functions C14orf43 had, and list some proteins which have the same functions with C14orf43. You can find most of the proteins on our site.

    Function Related Protein
    DNA binding PBX1A; PAX2; TIGD1; TFDP1B; ZNF19; MECOM; ZSCAN10; ZNF705B; AHR; SP1

    C14orf43 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 C14orf43 here. Most of them are supplied by our site. Hope this information will be useful for your research of C14orf43.

    HDAC1; HDAC2; DNTTIP1; ESR1; ESR2; MAPK14; mdm2_human_probe; SEC16A; DPM1; NDUFA10; MYC; PFKM

    Gallagher, MD; Suh, ER; et al. TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions. ACTA NEUROPATHOLOGICA 127:407-418(2014).
    van Blitterswijk, M; van Es, MA; et al. Evidence for an oligogenic basis of amyotrophic lateral sclerosis. HUMAN MOLECULAR GENETICS 21:3776-3784(2012).

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