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Rabbit Anti-GPR162  antibody (bs-15386R)  
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說明書: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價

產(chǎn)品編號 bs-15386R
英文名稱 Rabbit Anti-GPR162  antibody
中文名稱 G蛋白偶聯(lián)受體GPR162蛋白抗體
別    名 A 2; A-2; A2; G protein coupled receptor 162; Gene rich cluster gene A protein; Gene rich cluster, A; Gene-rich cluster gene A protein; GP162; GP162_HUMAN; GPR162; GRCA; Probable G protein coupled receptor 162; Probable G-protein coupled receptor 162.   
研究領域 細胞生物  免疫學  信號轉(zhuǎn)導  G蛋白偶聯(lián)受體  G蛋白信號  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse (predicted: Human,Rat,Rabbit,Pig,Sheep,Cow,Chicken,Dog,Horse)
產(chǎn)品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 64kDa
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human GPR162: 111-210/588 <Extracellular>
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 G protein-coupled receptors (GPRs), also known as seven transmembrane receptors, heptahelical receptors or 7TM receptors, comprise a superfamily of proteins that play a role in many different stimulus-response pathways. G protein coupled receptors translate extracellular signals into intracellular signals (G protein activation) and they respond to a variety of signaling molecules, such as hormones and neurotransmitters. GPR162 is a 588 amino acid multi-pass membrane protein that functions as an orphan receptor and belongs to the GPR1 family. Existing as two alternatively spliced isoforms, the gene encoding GPR162 maps to human chromosome 12p13.31. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

Function:
Orphan receptor.

Subcellular Location:
Cell membrane; Multi-pass membrane protein (By similarity).

Similarity:
Belongs to the G-protein coupled receptor 1 family.

SWISS:
Q16538

Gene ID:
27239

Database links:

Entrez Gene: 27239 Human

Entrez Gene: 14788 Mouse

SwissProt: Q16538 Human

SwissProt: Q3UN16 Mouse

Unigene: 631654 Human

Unigene: 2514 Mouse



產(chǎn)品圖片
Sample: Brain (Mouse) Lysate at 40 ug Primary: Anti-GPR162 (bs-15386R) at 1/300 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 64 kD Observed band size: 63 kD
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