CABP4 rabbit pAb
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],
Product Specifications
Background
UniProt
P57796
Swiss Prot
P57796
Reactivity
Human; Mouse
Immunogen
Synthesized peptide derived from part region of human protein
Target
CABP4
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
WB 1:500-2000 ELISA 1:5000-20000
Buffer
-20°C/1 year
Molecular Weight
30kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
30kD
Fragment
IgG
Subcellular 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
Available Sizes
Explore Other Products
Discover premium biology products from our extensive collection of 20M+ items