Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Trinucleotide Repeats, CAG, CACNA1A Gene

IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Trinucleotide Repeats, CAG, CACNA1A Gene

Definition : Molecular assay reagents intended to identify CAG repeats in the calcium channel, voltage-dependent, P/Q type, alpha 1A subunit (CACNA1A) gene, located at chromosome 19p13. Normal alleles have from 4 to 18 CAG repeats. A variation from the expected number of normal CAG trinucleotide repeat copies may produce altered DNA and improper gene functioning, resulting in full mutation. Alleles with 20 to 30 CAG trinucleotide repeats have been associated with spinocerebellar ataxia type 6 (SCA6).

Entry Terms : "Migraine Gene Mutation Reagents" , "Ataxia Gene Mutation Reagents" , "Familial Hemiplegic Migraine (FHM) Gene Mutation Reagents" , "Episodic Ataxia Type 2 (EA2) Gene Mutation Reagents" , "Spinocerebellar Ataxia Type 6 (SCA6) Gene Mutation Detection Reagents" , "CACNA1A Gene Mutation Detection Reagents, CAG Trinucleotide Repeats" , "Reagents, Molecular Assay, Gene Anomaly, Trinucleotide Repeats, CAG, CACNA1A Gene"

UMDC code : 25021

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