Anti-AIF抗体,调亡诱导因子抗体优质供应-上海研晶生物专业为您提供,欢迎咨询说明书等详细信息
来源:rabbit mouse
规格:0.1ml/0.2ml
产品类型 : 一抗 多抗; 产品价格:电询; 保存: Store at -20 °
:Apoptosis is characterized by several morphological nuclear changes including chromatin condensation and nuclear fragmentation. These changes are triggered by the activation of members of caspase family, caspase activated DNase, and several novel proteins. A novel gene, the product of which causes chromatin condensation and DNA fragmentation, was recently identified, cloned, and designated apoptosis inducing factor (AIF). Like the critical molecules, cytochrome c and caspase 9, in apoptosis, AIF localizes in mitochondria. AIF translocates to the nucleus when apoptosis is induced and induces mitochondria to release the apoptogenic proteins cytochrome c and caspase 9. AIF induces chromatin condensation and large scale DNA fragmentation, which are the hallmarks of apoptosis, of the isolated nucleus and the nucleus in live cells by microinjection and apoptosis stimuli. AIF is highly conserved between human and mouse and widely expressed.
( Not yet tested in other applications.Optimal dilutions/concentrations should be determined by the end user)
Anti-AIF抗体,调亡诱导因子抗体现货0.1ml;0.2ml,制备一般包括以下几个步骤:
1、制备抗原。
2、选择实验动物。
3、动物免疫。
4、试取血进行测试,看看是否成功免疫。
5、如果成功免疫,杀死实验动物,采集全部血清。
6、纯化出抗体。
7、鉴定抗体。包括纯度以及特异性
抗原修FF法:
化学方法
加热方法
水浴加热法
微波照射法
高压加热法
酸水解法
一抗是针对抗原的抗体,二抗是针对一抗的抗体。即抗体也可以充当抗原刺激机体产生抗体。
一抗体就是我们平时所说的抗体,它能和抗原特异性结合。
第二抗体是能和抗体结合,即抗体的抗体,其主要作用是检测抗体的存在。
蛋白质与多肽的联系:
多肽:通常由10~100氨基酸分子脱水缩合而成的化合物叫多肽,它们的分子量低于10,000Da(Dalton,道尔顿),能透过半透膜,不被三氯酸及硫铵所沉淀。也有文献把由2~10个氨基酸组成的肽称为寡肽(小分子肽);10~50个氨基酸组成的肽称为多肽;由50个以上的氨基酸组成的肽就称为蛋白质。
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Anti-AIF抗体,调亡诱导因子抗体进口优质抗体,现货目录供应,低价促销ing,公司销售各种类抗体,产品数量多,产品齐全,抗体纯化、抗体制备,公司权威提供技术支持。提供单克隆抗体制备、多克隆抗体制备、抗体标记服务。
技术文章:
多克隆抗体:
定义1:由多个B细胞克隆所产生的抗体,可与不同抗原表位结合且免疫球蛋白类别各异。
所属学科:免疫学(一级学科);免疫系统(二级学科);免疫分子(三级学科)
定义2:对特定抗原所产生的一组免疫球蛋白混合物,每种免疫球蛋白能识别抗原分子上的一个表位。
所属学科:生物化学与分子生物学(一级学科);总论(二级学科)
定义3:多种抗原表位刺激机体免疫系统后,机体产生的针对不同抗原表位的混合抗体。
所属学科:细胞生物学(一级学科);细胞免疫(二级学科)
ab1998 staining AIF in human U2OS cells by Immunocytochemistry/ Immunofluorescence.
Samples were fixed using 4% paraformaldehydeICC/IF image of ab1998 stained HeLa cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab1998, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.