OPN1MW antibody (N-Term)

Catalog No. ABIN5537021

This Rabbit Polyclonal antibody specifically detects OPN1MW in WB and FACS. It exhibits reactivity toward Human.

Quick Overview for OPN1MW antibody (N-Term) (ABIN5537021)

Target: OPN1MW (Opsin 1 (Cone Pigments), Medium-Wave-Sensitive (OPN1MW))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This OPN1MW antibody is un-conjugated

Application: Western Blotting (WB), Flow Cytometry (FACS)

Product Details anti-OPN1MW Antibody

Binding Specificity: AA 21-50, N-Term

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This OPN1MW antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 21-50 amino acids from the N-terminal region of human OPN1MW.

Isotype: Ig Fraction

Application Details

Application Notes: For WB starting dilution is: 1:1000

For FACS starting dilution is: 1:10~50

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Target Details for OPN1MW

Target: OPN1MW (Opsin 1 (Cone Pigments), Medium-Wave-Sensitive (OPN1MW))

Alternative Name: OPN1MW

Background: OPN1MW 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.

Molecular Weight: 41 kDa

Gene ID: 101060233, 2652, 728458

UniProt: P04001

Pathways: Phototransduction