本公司经销APP/ABPP，淀粉样肽前体蛋白抗体，克隆类型为polyclonal，宿主来源是Mouse，APP/ABPP淀粉样肽前体蛋白抗体可应用于WB、elisa、IP、IF、IHC等实验，欢迎垂询订购！

货号：BY-0112M
英文名称：Anti-APP/ABPP
中文名称：淀粉样肽前体蛋白抗体
其他名称：A4 amyloid protein; A4; AAA; ABETA; ABPP; AD 1; AD1; Alzheimer disease 1; Alzheimer disease; Alzheimer＇s disease amyloid protein; Amyloid beta （A4） precursor protein; Amyloid beta A4 protein; Amyloid beta A4 protein precursor isoform b; Amyloid beta A4 protein precursor isoform c; Amyloid beta A4 protein precursor isoform a; Amyloid beta A4 protein precursor isoform b; Amyloid beta A4 protein precursor isoform c; Amyloid beta protein; Amyloid beta-peptide; Amyloid of aging ａnd alzheimer disease; APP; APP I; APPI; Beta amyloid peptide; Cerebral vascular amyloid peptide; CTFgamma; CVAP; Human mRNA for amyloid A4 precursor of Alzheimer＇s disease; PN 2; PN II; PN2; PreA4; Protease nexin II.
抗体来源：Mouse
克隆类型：polyclonal
蛋白分子量：predicted molecular weight: 76/85kDa
纯化方法：affinity purified by Protein A
交叉反应：hu, mo, rat, Rb, hrs, cow, dog, chk, pig
产品介绍：Amyloid Precursor Protein （APP） functions as a cell surface kinesin I membrane receptor, mediating the axonal transport of beta-secretase ａnd presenilin 1. APP is important for neurite growth, neuronal adhesion ａnd axonogenesis. Immature APP （N-glycosylated in the endoplasmic reticulum） moves to the Golgi complex where complete maturation occurs （O-glycosylated ａnd sulfated）. After alpha-secretase cleavage, soluble APP is released into the extracellular space ａnd the C-terminal is internalized to endosomes ａnd lysosomes. Some APP accumulates in secretory transport vesicles leaving the late Golgi compartment ａnd returns to the cell surface. APP is expressed in the brain, kidney, heart ａnd spleen of fetal tissues; it is induced during neuronal differentiation. In adult brain, highest expression of APP is found in the frontal lobe of the cortex ａnd in the anterior perisylvian cortex-opercular gyri. Moderate expression in the cerebellar cortex, the posterior perisylvian cortex-opercular gyri ａnd the temporal associated cortex. Defects in APP are a cause of autosomal dominant Alzheimer＇s disease （AD）. APP695 （Amyloid protein precursor）淀粉样蛋白前体蛋白是一种大的细胞膜蛋白，其N端伸出于细胞外。该蛋白遭到破坏并释放出42个氨基酸的β-淀粉样肽，在老年斑和血管中被发现。这些异常蛋白可能积聚，而导致细胞失调和神经元的损伤。在研究APP与AD的关系中，该抗体十分重要。