IRTKS Polyclonal Antibody, 20ul Peptide Modification An autosomal recessive form of

An autosomal recessive form of juvenile amyotrophic lateral sclerosis was originally mapped to a region of chromosome 2 that includes ALS2CR11

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The protein encoded by ACO1 has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions

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IRTKS Polyclonal Antibody, 20ul Peptide Modification An autosomal recessive form ofBAIAP2L1 encodes a member of the IMD (IRSp53 MIM homology domain) family. Members of this family can be subdivided in two groups, the IRSp53 like and MIM like, based on the presence or absence of the SH3 (Src homology 3) domain. Brain specific angiogenesis inhibitor 1 associated protein 2 like protein 1 contains a conserved IMD, also known as F actin bundling domain, at the N terminus, and a canonical SH3 domain near the C terminus, so it belongs to