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TMC8 Polyclonal Antibody, 20ul Diagnostic Probes & Oligos KCNT1 (potassium sodium-activated channel subfamily

SKU: 58780388928

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TMC8 Polyclonal Antibody, 20ul Diagnostic Probes & Oligos KCNT1 (potassium sodium-activated channel subfamilyEpidermodysplasia verruciformis (EV) is an autosomal recessive dermatosis characterized by abnormal susceptibility to human papillomaviruses (HPVs) and a high rate of progression to squamous cell carcinoma on sun exposed skin. EV is caused by mutations in either of two adjacent genes located on chromosome 17q25. Both of these genes encode integral membrane proteins that localize to the endoplasmic reticulum and are predicted to form transmembrane

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Description

KCNT1 (potassium sodium-activated channel subfamily T member 1) encodes a sodium-activated potassium channel subunit which is thought to function in ion conductance and developmental signaling pathways

ITIH1 encodes a member of the inter-alpha-trypsin inhibitor family of proteins

SERPINA11 (Serpin Family A Member 11) is a Protein Coding gene

Mutations in this gene may be associated with dentinogenesis imperfect and autosomal dominant amylogenesis imperfect

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TMC8 Polyclonal Antibody, 20ul Diagnostic Probes & Oligos KCNT1 (potassium sodium-activated channel subfamilyEpidermodysplasia verruciformis (EV) is an autosomal recessive dermatosis characterized by abnormal susceptibility to human papillomaviruses (HPVs) and a high rate of progression to squamous cell carcinoma on sun exposed skin. EV is caused by mutations in either of two adjacent genes located on chromosome 17q25. Both of these genes encode integral membrane proteins that localize to the endoplasmic reticulum and are predicted to form transmembrane

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