OPN1MW rabbit monoclonal antibody
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Specification
Product Description
Rabbit monoclonal antibody raised against a human OPN1MW peptide using ARM Technology.
Immunogen
A synthetic peptide of human OPN1MW is used for rabbit immunization.
Customer or Abnova will decide on the preferred peptide sequence.Host
Rabbit
Library Construction
Non-fusion antibody library from rabbit spleen (ARM Technology).
Expression
Overexpression vector and transfection into 293H cell line.
Reactivity
Human
Purification
Protein A
Isotype
IgG
Quality Control Testing
Antibody reactive against human OPN1MW peptide by ELISA and mammalian transfected lysate by Western Blot.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
Deliverable
Up to three rabbit IgG clones of 100 ug each will be delivered to customer.
Note
1. Customer may provide cell or tissue lysate for antibody screening.
2. Rabbit monoclonal antibody generated by ARM technology is amenable to antibody engineering including F(ab)2, IgG, scFv and different Fc and non-Fc conjugates per customer request. -
Applications
Western Blot (Transfected lysate)
ELISA
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Gene Info — OPN1MW
Entrez GeneID
2652GeneBank Accession#
OPN1MWGene Name
OPN1MW
Gene Alias
CBBM, CBD, GCP, MGC176615, OPN1MW1
Gene Description
opsin 1 (cone pigments), medium-wave-sensitive
Gene Ontology
HyperlinkGene Summary
This gene 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. [provided by RefSeq
Other Designations
OTTHUMP00000024237|color blindness, deutan|green cone photoreceptor pigment|green cone pigment|opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan)|photopigment apoprotein
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