ABflo® 594 Rabbit anti-Human OPN1LW/OPN1MW mAb (100 T)

ABflo® 594 Rabbit anti-Human OPN1LW/OPN1MW mAb (100 T)

Brand: Abclonal
Cat. #: A24372
Availability: In Stock
$290.00
-+
Reactivity: Human    
Applications: FC    
Host Species: Rabbit    
Isotype: IgG    
Clonality: Monoclonal Antibody    
Conjugation: ABflo® 594. Ex:588nm. Em:604nm.
Gene Name: opsin 1, medium wave sensitive
Gene Symbol: OPN1MW
Synonyms: CBD; GCP; GOP; CBBM; COD5; OPN1MW1
Gene ID: 5956/2652
UniProt ID: P04000/P04001
Clone ID: 1Y8C6
Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-48 of human OPN1LW/OPN1MW (NP_064445.2).
Dilution: FC,5 μl per 10^6 cells in 100 μl volume
Purification Method: Affinity purification
Concentration: 0.01 mg/mL
Buffer: PBS with 0.03% proclin300,0.2% BSA, pH7.3.
Storage: Store at -20°C. Avoid freeze / thaw cycles.
Documents: Manual-OPN1MW antibody




Background

This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called red cone photopigment or long-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. This gene and the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of partial, protanopic colorblindness. This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called green cone photopigment or medium-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. The long-wavelength opsin gene and multiple copies of the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of deutanopic colorblindness.




Images

OPN1MW antibodyFlow cytometry: 1×10^6 293F cells (negative control,left) and 293F (Transfection,right) cells were surface-stained with ABflo® 594 Rabbit anti-Human OPN1LW/OPN1MW mAb (A24372,5 μl/Test,orange line) or ABflo® 594 Rabbit IgG isotype control (A23821,5 μl/Test,blue line). Non-fluorescently stained cells were used as blank control (red line).
Flow cytometry: 1×10^6 293F cells (negative control,left) and 293F (Transfection,right) cells were surface-stained with ABflo® 594 Rabbit anti-Human OPN1LW/OPN1MW mAb (A24372,5 μl/Test,orange line) or ABflo® 594 Rabbit IgG isotype control (A23821,5 μl/Test,blue line). Non-fluorescently stained cells were used as blank control (red line).
Flow cytometry: 1×10^6 293F (Transfection) cells were surface-stained with ABflo® 594 Rabbit IgG isotype control (A23821,5 μl/Test,left) or ABflo594 Human Rabbit anti-OPN1LW/OPN1MW mAb (A24372,5 μl/Test,right).
Flow cytometry: 1×10^6 293F (Transfection) cells were surface-stained with ABflo® 594 Rabbit IgG isotype control (A23821,5 μl/Test,left) or ABflo594 Human Rabbit anti-OPN1LW/OPN1MW mAb (A24372,5 μl/Test,right).



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