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RPAC2 Polyclonal Antibody, 100ul Modification Enzymes characterized by the lack of

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RPAC2 Polyclonal Antibody, 100ul Modification Enzymes characterized by the lack ofThe protein encoded by this gene is a component of the RNA polymerase I and RNA polymerase III complexes, which function in the synthesis of ribosomal RNA precursors and small RNAs, respectively. Mutations in this gene are a cause of Treacher Collins syndrome (TCS), a craniofacial development disorder. Alternative splicing results in multiple transcript variants.

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Description

characterized by the lack of the A subunit alone

This gene encodes a member of the proteasome B-type family| also known as the T1B family| that is a 20S core beta subunit

The protein is a replication-independent histone that is a member of the histone H3 family

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Mucin-1 is proteolytically cleaved into alpha and beta subunits that form a heterodimeric complex

RPAC2 Polyclonal Antibody, 100ul Modification Enzymes characterized by the lack ofThe protein encoded by this gene is a component of the RNA polymerase I and RNA polymerase III complexes, which function in the synthesis of ribosomal RNA precursors and small RNAs, respectively. Mutations in this gene are a cause of Treacher Collins syndrome (TCS), a craniofacial development disorder. Alternative splicing results in multiple transcript variants.

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