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KBTBA Rabbit Polyclonal Antibody, 100ul Antibody Humanization Loss of function of this

SKU: 57313374280

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KBTBA Rabbit Polyclonal Antibody, 100ul Antibody Humanization Loss of function of thisThis gene is a member of the kelch like family. The encoded protein contains a BACK domain a BTB POZ domain and 5 Kelch repeats. This protein is thought to function in skeletal muscle development and maintenance. Mutations in this gene have been associated with nemaline myopathy (NM) a rare congenital muscle disorder.

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Description

Loss of function of this gene is thought to contribute to cancer progression by increasing proliferation

GSC2 is expressed in a limited number of adult tissues

under certain conditions

Porphyria cutanea tarda

KBTBA Rabbit Polyclonal Antibody, 100ul Antibody Humanization Loss of function of thisThis gene is a member of the kelch like family. The encoded protein contains a BACK domain a BTB POZ domain and 5 Kelch repeats. This protein is thought to function in skeletal muscle development and maintenance. Mutations in this gene have been associated with nemaline myopathy (NM) a rare congenital muscle disorder.

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