Mtmr10

  • Official Full Name

    myotubularin related protein 10
Cat.# Product name Source (Host) Species Tag Protein Length Price
MTMR10-10202M Recombinant Mouse MTMR10 Protein Mammalian Cells Mouse His
MTMR10-4792Z Recombinant Zebrafish MTMR10 Mammalian Cells Zebrafish His
MTMR10-5714H Recombinant Human MTMR10 Protein, GST-tagged Wheat Germ Human GST
MTMR10-5785M Recombinant Mouse MTMR10 Protein, His (Fc)-Avi-tagged HEK293 Mouse His&Fc&Avi
MTMR10-5785M-B Recombinant Mouse MTMR10 Protein Pre-coupled Magnetic Beads HEK293 Mouse
MTMR10-6534HF Recombinant Full Length Human MTMR10 Protein, GST-tagged In Vitro Cell Free System Human GST Full L. 777 amino acids

    Involved Pathway

    Mtmr10 involved in several pathways and played different roles in them. We selected most pathways Mtmr10 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with Mtmr10 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

    Pathway Name Pathway Related Protein

    Protein Function

    Mtmr10 has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by Mtmr10 itself. We selected most functions Mtmr10 had, and list some proteins which have the same functions with Mtmr10. You can find most of the proteins on our site.

    Function Related Protein

    Interacting Protein

    Mtmr10 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 Mtmr10 here. Most of them are supplied by our site. Hope this information will be useful for your research of Mtmr10.

    Resources

    References

    • Le Pichon, JB; Yu, SH; et al. Genome-wide gene expression in a patient with 15q13.3 homozygous microdeletion syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS 21:1093-1099(2013).
    • Valbonesi, S; Magri, C; et al. Copy number variants in attention-deficit hyperactive disorder: identification of the 15q13 deletion and its functional role. PSYCHIATRIC GENETICS 25:59-70(2015).

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