Opsin 1, Short Wave Sensitive (OPN1SW) Antibody (HRP)
169€ (20 µg)
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935106861
info@markelab.com
name
Opsin 1, Short Wave Sensitive (OPN1SW) Antibody (HRP)
category
Primary Antibodies
provider
Abbexa
reference
abx337679
tested applications
ELISA
Description
OPN1SW Antibody (HRP) is a Rabbit Polyclonal against OPN1SW.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Opsin 1, Short Wave Sensitive (OPN1SW) |
| Host | Rabbit |
| Reactivity | Human |
| Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | HRP |
| Isotype | IgG |
| Purity | > 95% |
| Purification | Purified by Protein G. |
| Size 1 | 20 µg |
| Size 2 | 50 µg |
| Size 3 | 100 µg |
| Size 4 | 200 µg |
| Size 5 | 1 mg |
| Form | Liquid |
| Tested Applications | ELISA |
| Buffer | 0.01 M PBS, pH 7.4, 0.03% Proclin-300 and 50% Glycerol. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid exposure to light. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | P03999 |
| Gene ID | 611 |
| Alias | OPN1SW,opsin 1,short wave sensitive,opsin 1 (cone pigments) short-wave-sensitive (color blindness, tritan),opsin 1,opsin 1 (cone pigments),BCP,BOP,CBT |
| Background | Antibody anti-OPN1SW |
| Status | RUO |
Descripción
OPN1SW is an opsin found in the cone cells of the retina, responsible for detecting short wavelengths of light, typically in the blue region of the visible spectrum. It is activated by light with wavelengths ranging from approximately 420–440 nm. OPN1SW plays a crucial role in human color vision, particularly in the perception of blue hues. Like other opsins, OPN1SW works by converting light into an electrical signal that is sent to the brain for processing. This opsin is essential for maintaining the trichromatic vision system in humans, which enables the discrimination of colors in the blue portion of the visible spectrum. Mutations in the OPN1SW gene can result in color vision deficiencies, such as blue-yellow color blindness, where individuals struggle to distinguish between blue and yellow hues. The study of OPN1SW is important for understanding visual perception and the genetic basis of color vision defects.
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