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ATMIN Rabbit Polyclonal Antibody, 100ul Peptide Library Mutations in PMS1 cause hereditary

SKU: 52071277409

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ATMIN Rabbit Polyclonal Antibody, 100ul Peptide Library Mutations in PMS1 cause hereditary

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Description

Mutations in PMS1 cause hereditary nonpolyposis colorectal cancer type 3 (HNPCC3) either alone or in combination with mutations in other genes involved in the HNPCC phenotype

These receptors include members of the integrin family

Metallocarboxypeptidase that mediates deglutamylation of target proteins

The protein encoded by PRKAB1 (protein kinase AMP-activated non-catalytic subunit beta 1) is a regulatory subunit of the AMP-activated protein kinase (AMPK)

ATMIN Rabbit Polyclonal Antibody, 100ul Peptide Library Mutations in PMS1 cause hereditary

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