Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep,
适应物种:
Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep,
免疫原:
详见说明书
亚型:
IGg
形态:
粉末、液体、冻干粉
应用范围:
ICC=1:50-200 IF=1:50-200
浓度:
1mg/ml
保存条件:
-20 °C
规格:
100ul
FITC标记的G蛋白偶联受体GPR162蛋白抗体
英文名称
Anti-GPR162/FITC
中文名称
FITC标记的G蛋白偶联受体GPR162蛋白抗体
别 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.
规格价格
100ul/2980元 购买 大包装/询价
说 明 书
100ul
研究领域
细胞生物 免疫学 信号转导 G蛋白偶联受体 G蛋白信号
抗体来源
Rabbit
克隆类型
Polyclonal
交叉反应
Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep,
产品应用
ICC=1:50-200 IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
分 子 量
64kDa
性 状
Lyophilized or Liquid
浓 度
1mg/ml
免 疫 原
KLH conjugated synthetic peptide derived from human GPR162
亚 型
IgG
纯化方法
affinity purified by Protein A
储 存 液
0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件
Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
产品介绍
background: 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.
Database links:
Entrez Gene: 27239 Human
Entrez Gene: 14788 Mouse
SwissProt: Q16538 Human
SwissProt: Q3UN16 Mouse
Unigene: 631654 Human
Unigene: 2514 Mouse
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.