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CKAP2L

  • Official Full Name

    cytoskeleton associated protein 2-like

  • Synonyms

    CKAP2L;cytoskeleton associated protein 2-like;26877;ENSG00000169607;2q13;FLJ40629, MGC39683;cytoskeleton-associated protein 2-like;cytoskeleton-associated protein 2-like;
Species Cat.# Product name Source (Host) Tag Protein Length Price
Human CKAP2L-11260H Recombinant Human CKAP2L, His-tagged E.coli His 396-745a.a.
Mouse CKAP2L-3491M Recombinant Mouse CKAP2L Protein Mammalian Cell His
Mouse CKAP2L-1704M Recombinant Mouse CKAP2L Protein, His (Fc)-Avi-tagged HEK293 His (Fc)-Avi
Mouse CKAP2L-1704M-B Recombinant Mouse CKAP2L Protein Pre-coupled Magnetic Beads HEK293
  • CKAP2L Related Articles

CKAP2L involved in several pathways and played different roles in them. We selected most pathways CKAP2L participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with CKAP2L were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

Pathway Name Pathway Related Protein

CKAP2L has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by CKAP2L itself. We selected most functions CKAP2L had, and list some proteins which have the same functions with CKAP2L. You can find most of the proteins on our site.

Function Related Protein

CKAP2L 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 CKAP2L here. Most of them are supplied by our site. Hope this information will be useful for your research of CKAP2L.

Sapkota, Y; Low, SK; et al. Association between endometriosis and the interleukin 1A (ILIA) locus. HUMAN REPRODUCTION 30:239-248(2015).
Hussain, MS; Battaglia, A; et al. Mutations in CKAP2L, the Human Homo log of the Mouse Radmis Gene, Cause Filippi Syndrome. AMERICAN JOURNAL OF HUMAN GENETICS 95:622-632(2014).
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