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CABP4 Polyclonal Antibody, 100ul Microplate Mixer Defects in this gene may

SKU: 85012922277

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CABP4 Polyclonal Antibody, 100ul Microplate Mixer Defects in this gene mayThis gene encodes a member of the CABP family of calcium binding protein characterized by four EF hand motifs. Mutations in this gene are associated with congenital stationary night blindness type 2B. Three transcript variants encoding two different isoforms have been found for this gene.

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Description

Defects in this gene may be a cause of J-wave syndromes and sudden infant death syndrome (SIDS)

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that arises within the acrosomal vesicle during spermatogenesis

protein phosphatase 2

CABP4 Polyclonal Antibody, 100ul Microplate Mixer Defects in this gene mayThis gene encodes a member of the CABP family of calcium binding protein characterized by four EF hand motifs. Mutations in this gene are associated with congenital stationary night blindness type 2B. Three transcript variants encoding two different isoforms have been found for this gene.

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