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the most diverse group of intermediate filaments

Mutations in this gene cause Alexander disease

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It involves in translation termination in response to the termination codons UAA

SERCA1 Polyclonal Antibody, 20ul Custom DNA Oligos Take on any scientific challengeATP2A1 encodes one of the SERCA Ca(2+) ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen, and is involved in muscular excitation and contraction. Mutations in this gene cause some autosomal recessive forms of Brody disease, characterized by increasing