CABP4 rabbit pAb
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CABP4 rabbit pAb
Background :
This 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. [provided by RefSeq, Jul 2014]Description :
This 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. [provided by RefSeq, Jul 2014],UniProt :
P57796Swiss Prot :
P57796Reactivity :
Human; MouseImmunogen :
Synthesized peptide derived from part region of human proteinTarget :
CABP4Clonality :
PolyclonalSource :
RabbitApplications :
WB; ELISAConcentration :
1 mg/mlDilution :
WB 1:500-2000 ELISA 1:5000-20000Buffer :
-20°C/1 yearMolecular Weight :
30kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
30kDFragment :
IgGSubcellular Location :
Cytoplasm . Cell junction, synapse, presynapse . Found in rod spherules and cone pedicles of the presynapses from both types of photoreceptors. .Gene ID (Human) :
57010

