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PT117 Rabbit Polyclonal Antibody, 50ul Cell Function Analysis disease:Defects in NCF1 are the

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PT117 Rabbit Polyclonal Antibody, 50ul Cell Function Analysis disease:Defects in NCF1 are the

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Description

disease:Defects in NCF1 are the cause of chronic granulomatous disease autosomal recessive cytochrome-b-positive type 1 (CGD1)

They are involved in hormone biosynthesis

Translocation of this gene with PAX3 has been associated with alveolar rhabdomyosarcoma

The expression of this gene or the DUOX1 gene is not suppressed by thyroglobulin (Tg)| a macromolecular precursor in thyroid hormone synthesis| while the expression of the DUOX2 and DUOXA2 are significantly suppressed by the Tg

This gene encodes a member of the basic helix-loop-helix leucine zipper family

PT117 Rabbit Polyclonal Antibody, 50ul Cell Function Analysis disease:Defects in NCF1 are the

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