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RGR Rabbit pAb

-YT4069

主要信息
Target

RGR

Host Species

Rabbit

Reactivity

Human, Mouse

Applications

IHC, IF, ELISA

MW

32kD (Calculated)

Conjugate/Modification

Unmodified

货号: YT4069
规格
价格
货期
数量
200μL
¥3,780.00
现货

0

100μL
¥2,300.00
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0

40μL
¥960.00
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0

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详细信息
推荐稀释比
IHC 1:100-1:300; IF 1:200-1:1000; ELISA 1:5000; Not yet tested in other applications.
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
特异性
RGR Polyclonal Antibody detects endogenous levels of RGR protein.
纯化工艺
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
浓度
1 mg/ml
理论分子量
32kD
修饰
Unmodified
克隆性
Polyclonal
同种型
IgG
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抗原&靶点信息
免疫原:
The antiserum was produced against synthesized peptide derived from human RGR. AA range:169-218
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特异性:
RGR Polyclonal Antibody detects endogenous levels of RGR protein.
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基因名称:
RGR
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蛋白名称:
RPE-retinal G protein-coupled receptor
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别名:
RGR ;
RPE-retinal G protein-coupled receptor
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数据库链接:
Organism 基因 ID SwissProt
Human 5995; P47804;
Mouse Q9Z2B3;
背景:
retinal G protein coupled receptor(RGR) Homo sapiens This gene encodes a putative retinal G-protein coupled receptor. The gene is a member of the opsin subfamily of the 7 transmembrane, G-protein coupled receptor 1 family. Like other opsins which bind retinaldehyde, it contains a conserved lysine residue in the seventh transmembrane domain. The protein acts as a photoisomerase to catalyze the conversion of all-trans-retinal to 11-cis-retinal. The reverse isomerization occurs with rhodopsin in retinal photoreceptor cells. The protein is exclusively expressed in tissue adjacent to retinal photoreceptor cells, the retinal pigment epithelium and Mueller cells. This gene may be associated with autosomal recessive and autosomal dominant retinitis pigmentosa (arRP and adRP, respectively). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008],
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功能:
Disease:Defects in RGR are a cause of retinitis pigmentosa autosomal recessive (ARRP) [MIM:268000]. RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well.,Function:Receptor for all-trans- and 11-cis-retinal. Binds preferentially to the former and may catalyze the isomerization of the chromophore by a retinochrome-like mechanism.,online information:Retina International's Scientific Newsletter,PTM:Covalently binds all-trans- and 11-cis-retinal.,similarity:Belongs to the G-protein coupled receptor 1 family. Opsin subfamily.,tissue specificity:Preferentially expressed at high levels in the retinal pigment epithelium (RPE) and Mueller cells of the neural retina.,
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细胞定位:
Membrane; Multi-pass membrane protein.
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组织表达:
Preferentially expressed at high levels in the retinal pigment epithelium (RPE) and Mueller cells of the neural retina.
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货号: YT4069
规格
价格
货期
数量
200μL
¥3,780.00
现货

0

100μL
¥2,300.00
现货

0

40μL
¥960.00
现货

0

加入购物车

已收藏

收藏

定制服务咨询

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