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ADORA1 (基因名), Adenosine receptor A1 (蛋白名), AA1R_HUMAN.
产品名称:

Human ADORA1/ Adenosine receptor A1 CLIA Kit
腺苷受体A1

货号:

U12273h

商标:
EIAab®
监管等级:
检测方法:
CLIA
实验类型:
Sandwich
检测范围:
19.5-1250pg/mL
特异性:
Natural and recombinant human Adenosine receptor A1
样品类型:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
样品数据:
研究领域:
-
Human ADORA1 CLIA Kit
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产品说明书
说明书: 下载说明书
MSDS: MSDS


精密度

Intra-assay Precision (Precision within an assay):Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.

Intra-Assay CV: 3.9%

Inter-assay Precision (Precision between assays):Three samples of known concentration were tested in five separate assays to assess inter-assay precision.

Inter-Assay CV: 7.7%

回收率
Recovery was determined by spiking various levels of Adenosine receptor A1 into serum and plasma.

Sample Type

Average(%)

Recovery Range(%)

Serum

99

91-103

Plasma

98

93-106

 

 

 

 

线性
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Adenosine receptor A1 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Sample

1:2

1:4

1:8

1:16

serum(n=5)

92-105%

90-101%

95-105%

92-109%

EDTA plasma(n=5)

89-95%

93105%

89-94%

90-106%

heparin plasma(n=5)

93-104%

 

94-110%

101-111%

91-110%

 

通用注释


Sub Unit:
N/A


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


Subcellular Location:
Cell membrane Multi-pass membrane protein


该产品尚未在任何出版物中被引用。

[1].
"Cloning and functional characterization of a human A1 adenosine receptor."

[2].
"Mutation in ADORA1 identified as likely cause of early-onset parkinsonism and cognitive dysfunction."

[3].
"Association study of 182 candidate genes in anorexia nervosa."

[4].
"Physiogenomic analysis of statin-treated patients: domain-specific counter effects within the ACACB gene on low-density lipoprotein cholesterol?"

[5].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[6].
"Contribution of adenosine related genes to the risk of depression with disturbed sleep."

[7].
"Adenosine A1 receptor gene variants associated with post-traumatic seizures after severe TBI."

[8].
"Physiogenomic comparison of edema and BMI in patients receiving rosiglitazone or pioglitazone."

[9].
"Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study."

[10].
"Adenosine deaminase and adenosine receptor polymorphisms in aspirin-intolerant asthma."
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