Background:

CABP4 (Calcium Binding Protein 4) is a Protein Coding gene. Diseases associated with CABP4 include Cone-Rod Synaptic Disorder, Congenital Nonprogressive and Congenital Stationary Night Blindness, Type 2B. Among its related pathways are Visual Cycle in Retinal Rods. CABP4 encodes a member of the CABP family of calcium binding protein characterized by four EF-hand motifs. Mutations in CABP4 are associated with congenital stationary night blindness type 2B. Three transcript variants encoding two different isoforms have been found for CABP4.

Alternative names:

N/A

Clonality:

Polyclonal

Reactivity:

Human,Mouse

Source:

Rabbit

Isotype:

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Immunogen:

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Concentration:

1mg/ml

Applications:

WB, ELISA

Recommende dilutions:

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Storage:

PBS with 0.02% sodium azide and 50% glycerol pH 7.4. Store at -20°C. Avoid repeated freeze-thaw cycles.

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