OPN1SW Polyclonal antibody

OPN1SW Polyclonal Antibody for IF, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse

Applications

IF, ELISA

Conjugate

Unconjugated

Cat no : 24660-1-AP

Synonyms

Blue sensitive opsin, BOP, CBT, OPN1SW

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Validation Data Gallery

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  IF Staining of mouse eye using 24660-1-AP

  Immunofluorescent analysis of (4% PFA) fixed mouse eye tissue using OPN1SW antibody (24660-1-AP) at dilution of 1:200 and CoraLite®488-Conjugated AffiniPure Goat Anti-Rabbit IgG(H+L).

• 

  IF Staining of mouse eye using 24660-1-AP

  Immunofluorescent analysis of (4% PFA) fixed mouse eye tissue using OPN1SW antibody (24660-1-AP) at dilution of 1:200 and CoraLite®488-Conjugated AffiniPure Goat Anti-Rabbit IgG(H+L).

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Tested Applications

• Positive IF detected in: mouse eye tissue

Recommended dilution

• Immunofluorescence (IF): IF : 1:50-1:500

It is recommended that this reagent should be titrated in each testing system to obtain optimal results.

Sample-dependent, Check data in validation data gallery.

Product Information

24660-1-AP targets OPN1SW in IF, ELISA applications and shows reactivity with human, mouse samples.

• Tested Reactivity: human, mouse
• Host / Isotype: Rabbit / IgG
• Class: Polyclonal
• Type: Antibody
• Immunogen: OPN1SW fusion protein Ag20387
• Full Name: opsin 1 (cone pigments), short-wave-sensitive
• Calculated Molecular Weight: 348 aa, 39 kDa
• GenBank Accession Number: BC156719
• Gene Symbol: OPN1SW
• Gene ID (NCBI): 611
• Conjugate: Unconjugated
• Form: Liquid
• Purification Method: Antigen affinity purification
• Storage Buffer: PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
• Storage Conditions: Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20^oC storage. 20ul sizes contain 0.1% BSA.

Background Information

OPN1SW (Short-wave-sensitive opsin 1) belongs to the G-protein coupled receptor 1 family, opsin subfamily. It's one of three types of cone photoreceptors responsible for normal color vision. Inherited tritan color vision deficiencies exhibit an autosomal dominant inheritance pattern and are caused by mutations in OPN1SW (PMID: 32400513).