| 產(chǎn)品編號 | bsm-2011M-Gold |
| 英文名稱(chēng) | Mouse Anti-BCHE(1E8)/Gold Conjugated antibody |
| 中文名稱(chēng) | 膠體金標記的丁酰膽堿酯酶單克隆抗體 |
| 別 名 | Cholinesterase; Acylcholine acylhydrolase; Choline esterase II; CHE1; Butyrylcholine esterase; Pseudocholinesterase; butyrylcholinesterase. CHLE_HUMAN. |
| 規格價(jià)格 | 100ul/2980元 購買(mǎi) 大包裝/詢(xún)價(jià) |
| 說(shuō) 明 書(shū) | 100ul（10nm 15nm 35nm） |
| 研究領(lǐng)域 | 心血管 |
| 抗體來(lái)源 | Mouse |
| 克隆類(lèi)型 | Polyclonal |
| 克 隆 號 | 1E8 |
| 交叉反應 | (predicted: Human, ) |
| 產(chǎn)品應用 | IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 分 子 量 | 66kDa |
| 性 狀 | Lyophilized or Liquid |
| 濃 度 | 0.4mg/ml |
| 免 疫 原 | Full length native protein purified from human |
| 亞 型 | IgG |
| 純化方法 | affinity purified by Protein A |
| 儲 存 液 | 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300. |
| 保存條件 | Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles. |
| 產(chǎn)品介紹 |
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. Subcellular Location: Secreted. Tissue Specificity: Detected in blood plasma (at protein level). Present in most cells except erythrocytes. DISEASE: Butyrylcholinesterase deficiency (BChE deficiency) [MIM:177400]: 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. BChE deficiency is a multifactorial disorder. The hereditary condition is transmitted as an autosomal recessive trait. Note=The disease is caused by mutations affecting the gene represented in this entry. Similarity: Belongs to the type-B carboxylesterase/lipase family. 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. 血清丁酰膽堿酯酶是由四個(gè)亞基組成的糖蛋白，分子量28萬(wàn)～35萬(wàn)。作為一類(lèi)糖蛋白，主要存在于腦、肝、血及膽堿能神經(jīng)末稍的突觸間隙中，主要由肝臟合成，并存在于血清中，生理作用不明，稱(chēng)為假性膽堿酯酶或丁酰膽堿酯酶[1]Lockridge等采用Edman降解法測定了人血清BChE完整的氨基酸序列，共含有574個(gè)氨基酸殘基。BChE氨基酸序列與其他酯酶家族蛋白有很高的同源性。以電鰩AChE的三維結構為模板對人BChE的三維結構進(jìn)行計算機模擬結果表明，BChE活性中心，囊袋的底部為Ser198，其兩側相距一定距離分別是?；Y合部位和膽堿結合部位。研究發(fā)現人BChE的氨基酸序列上有Zn2+離子結合結構。 |
