SKU: WP17768 Categories: ,

SWS rabbit pAb

Price range: $268.00 through $328.00

SKU: WP17768-100
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Product details

Background:

This gene belongs to the G-protein coupled receptor 1 family, opsin subfamily. It encodes the blue cone pigment gene which is one of three types of cone photoreceptors responsible for normal color vision. Defects in this gene are the cause of tritan color blindness (tritanopia). Affected individuals lack blue and yellow sensory mechanisms while retaining those for red and green. Defective blue vision is characteristic. [provided by RefSeq, Jul 2008],

Specifications

Size50μL/100μL
TargetSWS
ReactivityHuman, Mouse, Rat
ApplicationsWB, ELISA, IHC
MW(Calculated)
MW(Observed)38kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000; IHC 1:50-300; ELISA 1:2000-20000 / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human SWS
SpecificityThis antibody detects endogenous levels of Human SWS
Gene NameOPN1SW BCP
Protein NameShort-wave-sensitive opsin 1 (Blue cone photoreceptor pigment) (Blue-sensitive opsin) (BOP)
Other NameShort-wave-sensitive opsin 1; / Blue cone photoreceptor pigment; / Blue-sensitive opsin; / BOP
SpeciesHuman
Gene ID611
UniprotP03999,
Species.1Mouse
Gene ID.112057
Uniprot.1P51491,
Species.2Rat
Gene ID.281644
Uniprot.2Q63652
Cellular LocalizationCell membrane; Multi-pass membrane protein . Photoreceptor inner segment . Cell projection, cilium, photoreceptor outer segment . Cytoplasm, perinuclear region .
Tissue ExpressionThe three color pigments are found in the cone photoreceptor cells (PubMed:2937147). Expressed throughout the epidermis and dermis, primarily in the stratum granulosum in the facial and abdominal skin (at protein level) (PubMed:30168605). Expressed in dermal fibroblasts (at protein level) (PubMed:31380578). Expressed in melanocytes (at protein level) (PubMed:31730232).
Signaling_pathway
Research Areas
FunctionDisease:Defects in OPN1SW are the cause of tritan color blindness (tritanopia) [MIM:190900].,Function:Visual pigments are the light-absorbing molecules that mediate vision. They consist of an apoprotein, opsin, covalently linked to cis-retinal.,online information:Retina International's Scientific Newsletter,PTM:Phosphorylated on some or all of the serine and threonine residues present in the C-terminal region.,similarity:Belongs to the G-protein coupled receptor 1 family.,similarity:Belongs to the G-protein coupled receptor 1 family. Opsin subfamily.,tissue specificity:The three color pigments are found in the cone photoreceptor cells.,
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