质量水平
检测方案
≥95% (HPLC)
形式
powder
UniProt登记号
储存温度
−20°C
SMILES字符串
CCC(C)C(NC(=O)CNC(=O)C(CC(C)C)NC(=O)C(N)CCSC)C(=O)NC(C(C)CC)C(=O)NC(C)C(=O)NCC(=O)NC(CCCCN)C(=O)NC(CC(N)=O)C(=O)NC(CO)C(=O)NCC(O)=O
InChI
1S/C45H81N13O14S/c1-9-24(5)36(57-34(62)20-50-40(67)29(17-23(3)4)54-39(66)27(47)14-16-73-8)45(72)58-37(25(6)10-2)44(71)52-26(7)38(65)49-19-33(61)53-28(13-11-12-15-46)42(69)55-30(18-32(48)60)43(70)56-31(22-59)41(68)51-21-35(63)64/h23-31,36-37,59H,9-22,46-47H2,1-8H3,(H2,48,60)(H,49,65)(H,50,67)(H,51,68)(H,52,71)(H,53,61)(H,54,66)(H,55,69)(H,56,70)(H,57,62)(H,58,72)(H,63,64)
InChI key
IDGOADDOQWKZOX-UHFFFAOYSA-N
基因信息
human ... APP(351)
Amino Acid Sequence
Met-Leu-Gly-Ile-Ile-Ala-Gly-Lys-Asn-Ser-Gly
一般描述
β淀粉样前体蛋白(APP)属于Ⅰ型跨膜蛋白。APP广泛表达,主要存在于突触与神经元中。APP基因位于人染色体 21q21.3。
应用
β淀粉样蛋白片段35-25可作为对照肽,用于Aβ诱导的细胞凋亡,研究铁调素过表达对小鼠β淀粉样蛋白诱导的大脑损伤的影响。
生化/生理作用
β淀粉样前体蛋白(APP)经水解形成β淀粉样蛋白(Aβ),沉积为阿尔茨海默病的主要生物标志物——大脑淀粉样斑块。APP参与神经发生、突触形成、轴突运输、神经元迁移和神经突生长。还参与线粒体相关内质网膜(MAM)活动、抗菌保护作用、胆固醇和铁稳态过程。β淀粉样蛋白片段35-25是失活对照。
其他说明
片段 25-35的N—C反向序列
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
常规特殊物品
Mechanisms of ageing and development, 196, 111477-111477 (2021-04-03)
Emerging evidence from experimental and clinical research suggests that stress-related genes may play key roles in AD development. The fact that genome-wide association studies were not able to detect a contribution of such genes to AD indicates the possibility that
Scientific reports, 11(1), 19115-19115 (2021-09-29)
Amyloid precursor protein (APP) is expressed in many tissues in human, mice and in zebrafish. In zebrafish, there are two orthologues, Appa and Appb. Interestingly, some cellular processes associated with APP overlap with cilia-mediated functions. Whereas the localization of APP
Alzheimer's disease: amyloid beta-peptide antibody vaccine as plaque remover.
Journal of biosciences, 25(4), 315-316 (2000-12-20)
Metabolic brain disease, 34(5), 1365-1374 (2019-07-04)
The amyloid β-peptide (Aβ) is transported across the blood-brain barrier (BBB) by binding with the receptor for advanced glycation end products (RAGE). Previously, we demonstrated that the Aβ fraction 25-35 (Aβ25-35) increases RAGE expression in the rat hippocampus, likely contributing
Cell death discovery, 6(1), 113-113 (2020-12-11)
Progressive iron accumulation in the brain and iron-induced oxidative stress are considered to be one of the initial causes of Alzheimer's disease (AD), and modulation of brain iron level shows promise for its treatment. Hepcidin expressed by astrocytes has been
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