OPN1MW antibody (N-Term)

Catalog No. ABIN651110

The Rabbit Polyclonal anti-OPN1MW antibody has been validated for WB and FACS. It is suitable to detect OPN1MW in samples from Human.

Quick Overview for OPN1MW antibody (N-Term) (ABIN651110)

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)

Clone: RB24518

Product Details anti-OPN1MW Antibody

Binding Specificity: AA 21-50, N-Term

Predicted Reactivity: Rat, C, X

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: WB: 1:1000. FC: 1:10~50

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody 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: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Expiry Date: 6 months

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: 40584

Gene ID: 728458

NCBI Accession: NP_000504, NP_001041646

UniProt: P04001

Pathways: Phototransduction