丁酰胆碱酯酶抗体
规格：1mg/1ml
英文名： Butyrylcholinesterase (NT)
别名： Cholinesterase; Acylcholine acylhydrolase; Choline esterase II; CHE1; BCHE; Butyrylcholine esterase; Pseudocholinesterase; butyrylcholinesterase. CHLE_HUMAN.
分子量： 66kDa
储存液：0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce
克隆类型：Polyclonal
亚型：IgG
纯化方法：affinity purified by Protein A
**原：KLH conjugated synthetic peptide derived from human BCHE
交叉反应：Human, Mouse, Rat, Cow,
细胞定位：分泌型蛋白
丁酰胆碱酯酶抗体产品介绍：background: Mutant alleles at the BCHE locus are responsible for suxamethonium sensitivity. Homozygous persons sustain prolonged apnea after administration of the muscle relaxant suxamethonium in connection with surgical anesthesia. The activity of pseudocholinesterase in the serum is low and its substrate behavior is atypical. In the absence of the relaxant, the homozygote is at no known disadvantage. [provided by RefSeq, Jul 2008]. Function: Esterase with broad substrate specificity. Contributes to the inactivation of the neurotransmitter acetylcholine. Can degrade neurotoxic organophosphate esters. Subunit: Homotetramer; disulfide-linked. Dimer of dimers.丁酰胆碱酯酶抗体 Subcellular Location: Secreted. Tissue Specificity: Detected in blood plasma (at protein level). Present in most cells except erythrocytes. DISEASE: Defects in BCHE are the cause of butyrylcholinesterase deficiency (BChE deficiency) [MIM:177400]. BChE deficiency is a metabolic disorder characterized by prolonged apnoea after the use of certain anesthetic drugs, including the muscle relaxants succinylcholine or mivacurium and other ester local anesthetics. The duration of the prolonged apnoea varies significantly depending on the extent of the enzyme deficiency. 丁酰胆碱酯酶抗体BChE deficiency is a multifactorial disorder. The hereditary condition is transmitted as an autosomal recessive trait. Similarity: Belongs to the type-B carboxylesterase/lipase family. Gene ID: 590 Database links: Entrez Gene: 590 Human Omim: 177400 Human SwissProt: P06276 Human Unigene: 420483 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 丁酰胆碱酯酶Bche又称假性胆碱酯酶。该酶主要分布于脑白质（中脑，桥脑，延脑，纹状体及丘脑等脑干区域），也分布于心血管系统、呼吸系统、消化系统等组织及腺体中，专一性水解丁酰胆碱酯而发挥其生理功能。目前有用于老年痴呆AD病方面的的研究。 （脊椎动物体内有两种胆碱酯酶：乙酰胆碱酯酶AchE，又叫真性胆碱酯酶。该酶不仅存在于胆碱能神经，也存在于非但碱能神经及其他组织，如胎盘、红细胞等，专一水解Ach；在一种就是丁酰胆碱酯酶Bche）
丁酰胆碱酯酶抗体产品应用：ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 （石蜡切片需做抗原修复） not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
研究领域：肿瘤 细胞生物 神经生物学 信号转导 Alzheimer's
储存条件： Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
来源： Rabbit
外观： Lyophilized or Liquid