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PSPC1 Polyclonal Antibody, 50ul Recombinant Protein Expression Mutations in DCLRE1C can cause

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PSPC1 Polyclonal Antibody, 50ul Recombinant Protein Expression Mutations in DCLRE1C can causeThis gene encodes a nucleolar protein that localizes to punctate subnuclear structures that occur close to splicing speckles, known as paraspeckles. These paraspeckles are composed of RNA protein structures that include a non coding RNA, NEAT1 Men epsilon beta, and the Drosophila Behavior Human Splicing family of proteins, which include the product of this gene and the P54NRB NONO and PSF SFPQ proteins. Paraspeckles may function in the control of gene

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Description

Mutations in DCLRE1C can cause Athabascan-type severe combined immunodeficiency (SCIDA) and Omenn syndrome

All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions

This protein is specific for the kidney

and mouse and appear to regulate cytoskeletal organization

I-1 is inactivated by calcineurin (or PP2B)

PSPC1 Polyclonal Antibody, 50ul Recombinant Protein Expression Mutations in DCLRE1C can causeThis gene encodes a nucleolar protein that localizes to punctate subnuclear structures that occur close to splicing speckles, known as paraspeckles. These paraspeckles are composed of RNA protein structures that include a non coding RNA, NEAT1 Men epsilon beta, and the Drosophila Behavior Human Splicing family of proteins, which include the product of this gene and the P54NRB NONO and PSF SFPQ proteins. Paraspeckles may function in the control of gene

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