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MAGI-2 Polyclonal Antibody, 50ul DNA Synthesis Mutations in GNPAT are associated

SKU: 73157793501

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SEK162.00 SEK203.00

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MAGI-2 Polyclonal Antibody, 50ul DNA Synthesis Mutations in GNPAT are associatedThe protein encoded by MAGI2 (membrane associated guanylate kinase, WW and PDZ domain containing 2)interacts with atrophin 1. Atrophin 1 contains a polyglutamine repeat, expansion of which is responsible for dentatorubral and pallidoluysian atrophy. This encoded protein is characterized by two WW domains, a guanylate kinase like domain, and multiple PDZ domains. It has structural similarity to the membrane associated guanylate kinase homologue (MAGUK)

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Description

Mutations in GNPAT are associated with rhizomelic chondrodysplasia punctata

The DNA-binding activity may reside exclusively on the 70 kDa subunit

This protein is a molecular chaperone with specific function in cell signal transduction

Composed of three domains: a modulating N-terminal domain| a DNA-binding domain and a C-terminal steroid-binding domain

The protein encoded by this gene is a DNA helicase that belongs to the RecQ helicase family

MAGI-2 Polyclonal Antibody, 50ul DNA Synthesis Mutations in GNPAT are associatedThe protein encoded by MAGI2 (membrane associated guanylate kinase, WW and PDZ domain containing 2)interacts with atrophin 1. Atrophin 1 contains a polyglutamine repeat, expansion of which is responsible for dentatorubral and pallidoluysian atrophy. This encoded protein is characterized by two WW domains, a guanylate kinase like domain, and multiple PDZ domains. It has structural similarity to the membrane associated guanylate kinase homologue (MAGUK)

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