ab15759 ADORA1 Antibody

Figure 6. |Density A1R and A2AR analysed by Western blot in nerve terminal-enriched membranes(A) and total membranes (B) from the hippocampus of GK and Wistar (W) rats, either receiving 1g/L caffeine (Caff) or tap water. Samples were loaded in SDS-PAGE gels at a protein concentration of 40 or 150 μg for A1R (n=6-8) and A2AR (n=2-3), respectively. Immunoreactivity was normalised to either α-tubulin or β-actin, and calculated as percentage of control in the same Western blot experiment. Symbols represent LSD test results after ANOVA with either significant diabetes effect or significant diabetes-caffeine interaction: *P<0.05, **P<0.01 for GK versus Wistar in the respective treatment group or as indicated.

品牌

产品货号

来源种属

Rabbit

抗体克隆

Polyclonal

来源亚型

IgG

实验方法

WB

实验种属

Human,Mouse,Rat,Rabbit,Pig,Dog,Chicken,Bovine,Horse,Sheep

偶联标记

Unconjugated

目的蛋白

ADORA1

产品规格

50μl,100μl,200μl

产品报价

¥1500/¥2750/¥3600

实验应用

Western blotting

Recommended dilution: 1:500-1:1000

 



最佳稀释倍数与浓度应由实验研究人员确认

产品说明



产品背景

Receptor for adenosine. The activity of this receptor is mediated by G proteins which inhibit adenylyl cyclase.

Description
Rabbit polyclonal antibody to ADORA1

Applications 
WB.

Immunogen 
ADORA1 Antibody detects endogenous levels of total ADORA1.

Reactivity 
Human, Rat.
可预测:Pig(83%), Horse(%), Rabbit(%)

Molecular weight
37 KD; 37kD(Calculated).

Host species 
Rabbit

Ig class 
Immunogen-specific rabbit IgG

Purification 
Antigen affinity purification

Full name 
ADORA1

Synonyms 
A1AR; A1R; AA1R; AA1R_HUMAN; Adenosine receptor A1; ADORA 1; ADORA 1; ADORA1; RDC 7; RDC7; Ri;

Storage
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.

Swissprot 
P30542

产品图片

Figure 6. |Density A1R and A2AR analysed by Western blot in nerve terminal-enriched membranes(A) and total membranes (B) from the hippocampus of GK and Wistar (W) rats, either receiving 1g/L caffeine (Caff) or tap water. Samples were loaded in SDS-PAGE gels at a protein concentration of 40 or 150 μg for A1R (n=6-8) and A2AR (n=2-3), respectively. Immunoreactivity was normalised to either α-tubulin or β-actin, and calculated as percentage of control in the same Western blot experiment. Symbols represent LSD test results after ANOVA with either significant diabetes effect or significant diabetes-caffeine interaction: *P<0.05, **P<0.01 for GK versus Wistar in the respective treatment group or as indicated.

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