OPN1MW anticorps (N-Term)

N° du produit ABIN651110

L’anticorps Lapin Polyclonal anti-OPN1MW a été validé pour WB et FACS. Il convient pour détecter OPN1MW dans des échantillons de Humain.

Aperçu rapide pour OPN1MW anticorps (N-Term) (ABIN651110)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp OPN1MW est non-conjugé

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

Clone: RB24518

Détail du produit anti-OPN1MW anticorps

Épitope: AA 21-50, N-Term

Homologie: Rat, C, X

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

Immunogène: 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

Information d'application

Indications d'application: WB: 1:1000. FC: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: 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.

Date de péremption: 6 months

Détails sur OPN1MW

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

Autre désignation: OPN1MW

Sujet: 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.

Poids moléculaire: 40584

ID gène: 728458

NCBI Accession: NP_000504, NP_001041646

UniProt: P04001

Pathways: Phototransduction