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首页  >  酶联免疫试剂盒  >  Mouse Ache ELISA Kit
Ache (基因名), Acetylcholinesterase (蛋白名), ACES_MOUSE.
产品名称:

Mouse Ache/ Acetylcholinesterase ELISA Kit
乙酰胆碱脂

货号:

E1195m

商标:
EIAab®
监管等级:
别名:

AChE

检测方法:
ELISA
实验类型:
Sandwich
检测范围:
0.78-50ng/mL
灵敏度:
0.402ng/mL
特异性:
Natural and recombinant mouse Acetylcholinesterase
样品类型:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
样品数据:
实验步骤:
实验步骤
研究领域:
Neurosciences
Mouse Ache ELISA Kit
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产品说明书
数据表: 下载说明书
说明书: 下载说明书
MSDS: MSDS


精密度
批内差:已知浓度的3个样本在一个板子内重复检测20次,以评估批内精密度。
批内 CV: ≤4.8%
批间差:已知浓度的3个样本在不同的板子上重复测定5次,以评估测定批间精密度。
批间 CV: ≤7.9%
回收率
回收率:低、中和高浓度的分析物被掺入到血清或者血浆样本中,进行回收实验测定。

Sample Type

Average(%)

Recovery Range(%)

Serum

100

94-106

Plasma

102

96-108

 

 

 

 

线性
线性:给定样本通过梯度稀释,每次稀释的测量值与理论值的比值。

Sample

1:2

1:4

1:8

1:16

serum(n=5)

90-100%

96-106%

92-101%

94-103%

EDTA plasma(n=5)

84-95%

97-107%

110-120%

103-112%

heparin plasma(n=5)

91-103%

 

80-89%

96-105%

85-97%

 

通用注释


亚单元:
Isoform H generates GPI-anchored dimers; disulfide linked. Isoform T generates multiple structures, ranging from monomers and dimers to collagen-tailed and hydrophobic-tailed forms, in which catalytic tetramers are associated with anchoring proteins that attach them to the basal lamina or to cell membranes. In the collagen-tailed forms, isoform T subunits are associated with a specific collagen, COLQ, which triggers the formation of isoform T tetramers, from monomers and dimers (By similarity). Interacts with PRIMA1. The interaction with PRIMA1 is required to anchor it to the basal lamina of cells and organize into tetramers.


功能:
Terminates signal transduction at the neuromuscular junction by rapid hydrolysis of the acetylcholine released into the synaptic cleft.


亚细胞位置:
Isoform H Cell membrane Lipid-anchor GPI-anchor Extracellular side


该产品尚未在任何出版物中被引用。

[1].
"Variability of AChE, BChE, and ChAT genes in the late-onset form of Alzheimer's disease and relationships with response to treatment with Donepezil and Rivastigmine."

[2].
"Structures of recombinant native and E202Q mutant human acetylcholinesterase complexed with the snake-venom toxin fasciculin-II."

[3].
"Expression of three alternative acetylcholinesterase messenger RNAs in human tumor cell lines of different tissue origins."

[4].
"Mutagenesis of human acetylcholinesterase. Identification of residues involved in catalytic activity and in polypeptide folding."

[5].
"Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia."

[6].
"Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients."

[7].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[8].
"Physiogenomic analysis of statin-treated patients: domain-specific counter effects within the ACACB gene on low-density lipoprotein cholesterol?"

[9].
"Structural evidence that human acetylcholinesterase inhibited by tabun ages through O-dealkylation."

[10].
"Donepezil, a potent acetylcholinesterase inhibitor, induces caspase-dependent apoptosis in human promyelocytic leukemia HL-60 cells."
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