OPN1SW (Human) Recombinant Protein
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Specification
Product Description
Human OPN1SW full-length ORF (AAI56720.1) recombinant protein without tag.
This product is belong to Proteoliposome (PL).Sequence
MRKMSEEEFYLFKNISSVGPWDGPQYHIAPVWAFYLQAAFMGTVFLIGFPLNAMVLVATLRYKKLRQPLNYILVNVSFGGFLLCIFSVFPVFVASCNGYFVFGRHVCALEGFLGTVAGLVTGWSLAFLAFERYIVICKPFGNFRFSSKHALTVVLATWTIGIGVSIPPFFGWSRFIPEGLQCSCGPDWYTVGTKYRSESYTWFLFIFCFIVPLSLICFSYTQLLRALKAVAAQQQESATTQKAEREVSRMVVVMVGSFCVCYVPYAAFAMYMVNNRNHGLDLRLVTIPSFFSKSACIYNPIIYCFMNKQFQACIMKMVCGKAMTDESDTCSSQKTEVSTVSSTQVGPN
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
38.28
Interspecies Antigen Sequence
Mouse (86)
Form
Liquid
Preparation Method
in vitro wheat germ expression system with proprietary liposome technology
Purification
None
Recommend Usage
Heating may cause protein aggregation. Please do not heat this product before electrophoresis.
Storage Buffer
25 mM Tris-HCl of pH8.0 containing 2% glycerol.
Storage Instruction
Store at -80°C. Aliquot to avoid repeated freezing and thawing.
Note
Best use within three months from the date of receipt of this protein.
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Applications
Antibody Production
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Gene Info — OPN1SW
Entrez GeneID
611GeneBank Accession#
BC156719.1Protein Accession#
AAI56720.1Gene Name
OPN1SW
Gene Alias
BCP, BOP, CBT
Gene Description
opsin 1 (cone pigments), short-wave-sensitive
Omim ID
190900Gene Ontology
HyperlinkGene Summary
This gene belongs to the G-protein coupled receptor 1 family, opsin subfamily. It encodes the blue cone pigment gene which is one of three types of cone photoreceptors responsible for normal color vision. Defects in this gene are the cause of tritan color blindness (tritanopia). Affected individuals lack blue and yellow sensory mechanisms while retaining those for red and green. Defective blue vision is characteristic. [provided by RefSeq
Other Designations
blue cone photoreceptor pigment|blue-sensitive opsin
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Interactome
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Disease
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