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CD6 Polyclonal Antibody, 50ul[BT-AP01864] Cellular Function Assays Several transcript variants encoding the

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CD6 Polyclonal Antibody, 50ul[BT-AP01864] Cellular Function Assays Several transcript variants encoding theThe product of CLCN7 belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. CLCN7 encodes chloride channel 7. Defects in CLCN7 are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers

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Description

Several transcript variants encoding the same protein have been found for TNFAIP3

The protein encoded by this gene is a transcriptional repressor thought to negatively regulate MYC function

FXYD3 (MAT-8)

There are numerous pseudogenes of this gene distributed throughout the genome

This gene is a member of the Antp homeobox family and encodes a protein with a homeobox DNA-binding domain

CD6 Polyclonal Antibody, 50ul[BT-AP01864] Cellular Function Assays Several transcript variants encoding theThe product of CLCN7 belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. CLCN7 encodes chloride channel 7. Defects in CLCN7 are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers

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