AbC™AntiMouseBeadKit
实验概要The AbC™ Anti-Mouse Bead Kit provides a consistent, accurate, and simple-to-use technique for the setting of flow cytometry compensation when using fluorochrome-conjugated mouse antibodies (Picture 1). The kit contains two types of specially modified polystyrene microspheres, the AbC™ capture beads, that bind all isotypes of mouse immunoglobulin, and the negative beads that hav......阅读全文
AbC™－AntiMouse－Bead－Kit
实验概要The AbC™ Anti-Mouse Bead Kit provides a consistent, accurate, and simple-to-use technique for the setting of flow cytometry compensation when u
AbC™－AntiMouse－Bead－Kit
实验概要The AbC™ Anti-Mouse Bead Kit provides a consistent, accurate, and simple-to-use technique for the setting of flow cytometry compensation when u
Th17－Polarization－of－Mouse－CD4－Cells
实验概要T helper 17 (Th17) cells are a subset of CD4 T helper cells characterized by their production of IL-17, particularly IL-17A and IL-17F. They are
Th9－Polarization－of－Mouse－Splenocytes
实验概要Th9 cells are a subpopulation of T-helper cells, characterized to be involved in allergic diseases and resistance against intestinal nematodes.
Immunofluorescent－staining－of－Sea－Urchin－embryos
1. Transfer fixed embryos to microfuge tubes. Allow to settle for 10 minutes.Gently remove most of the liquid.2. Add 100 ul antibody to one tube and 1
ImmunohistochemistyFluorescence－Protocol1
MaterialsCytokine-specific Primary Antibodiesunlabeled or biotinylated antigen-affinity purified polyclonal antibodies (R&D Systems ''AF'&
3－Color－Staining:－AlphaCatenin－in－HeLa－Human－Cervical－Cancer－Cells
实验概要Alpha-catenin in HeLa human cervical cancer cells was labeled using mouse anti-α-catenin and visualized with Alexa Fluor® 488 goat anti-mouse Ig
二抗的选择和定位
第一步：选择抗体。三种二抗抗体：Whole IgG，F(ab&；rsquo；)2片段，Fab片段。 Whole IgG抗体适用于多数情况，是性价比最高的。Whole IgG是完整的抗体分子，有一个Fc部分和两个与抗原结合的Fab部分 (Figure 1, Jackson ImmunoResearch
Immunodetection－of－cyclin－D1－and－D2/D3－using－flow－cytometry
DescriptionThis protocol is for use with the D cyclins and employs 488 nm argon laser excitation of propidium iodide and 630 nm NeNe or diode laser ex
二抗的选择
二抗应选用与使用的一抗相同的物种来源，例如：如果你的一抗是小鼠的单克隆抗体，二抗则选抗小鼠的二抗anti-mouse secondary。建议检查二抗说明书确保该抗体适用于你的检测应用， 二抗一般连接荧光素FITC或发光团。
ALKALINE－PHOSPHATASE－(APAAP)－TECHNIQUE
Preparation: Cytological PreparationsFixation: Air dry films or cytospin preparations overnight at room temperature. For frozen and paraffin sections
小鼠Treg检测操作步骤
1、在每个流式上样管中加入100 µl准备好的细胞悬液，细胞数约为1x106个.2、按照细胞表面抗原染色方法标记表面抗原。根据说明书加入CD4和CD25抗体100 µl体系中使用0.125 µg FITC anti-mouse CD4，0.06 µg APC anti-mouse CD25抗体。最好
Early－development－of－primary－motor－neurons－and－somites－in－Zebrafish－Embryos
Background:Zebrafish,or the teleost fish Danio rerio,is a rapidly developing organism that is apopular species for studying vertebrate development. Cl
Cell－Surface－Immunofluorescence－Staining－Protocol
实验概要A method of identifying and enumerating specific cell types in a heterogeneous population of cells by enhancing the specific staining of desired
间标磁珠——轻松分选任意细胞
我们知道，做细胞分选，首先要知道目的细胞与其它细胞相比，有什么特别的标志，如常用的细胞表面CD marker，最简单的方法是选择直接耦联相应抗体的磁珠，即所谓的直标微珠，如用CD4 microbeads来直接分选CD4 + T细胞。 但是，美天旎的直标磁珠多是针对小鼠、大鼠、人和灵长类的，针对其它物
Brdu免疫组织化学染色分析－BrdU－incorporation－assay
Enzyme Immunostaining for BrdU:Wash frozen sections with PBS 2x.Put them in 0.1% Pepsin in 0.1N HCL (in PBS) at 37�C for 50min.Then in 0.3% hydrogen p
LIVE/DEAD®－Fixable－Dead－Cell－Stain－Kits
实验概要The LIVE/DEAD® Fixable Dead Cell Stain Kits use a novel method to evaluate the viability of mammalian cells by flow cytometry. These assays are
Indirect－ELISA
实验概要 In the indirect ELISA, the enzyme-antibody conjugate uses an antibody against the type of antibody that is used to detect the antigen, kind of
specific－immunodetection－of－cyclins－using－488/630－dual－laser－flow－cytometry
Phenotype-specific immunodetection of cyclins using 488/630 nm dual laser flow cytometryWilliam Telford Hospital for Special SurgeryThis protocol is f
Immunohistochemistry－using－AntiGanglioside－Antibodies
Immunohistochemistry using Anti-Ganglioside AntibodiesTadashi Tai~Head, Department of Tumor Immunology, The Tokyo Metropolitan Institute of Medical Sc
LIVE/DEAD®－Fixable－Dead－Cell－Stain－Kits
实验概要The LIVE/DEAD® Fixable Dead Cell Stain Kits use a novel method to evaluate the viability of mammalian cells by flow cytometry. These assays are
ELISA－with－Platelet
OUTLINEThis modification of qualitative ELISA (Enzyme-Linked Immunosorbent Assay) is used for either screening detection of anti-platelet antibodies o
Wholemount－staining－of－embryos
Fix embryos in formalin or MEMFA for one hour at room temperature with mixing. Rinse with TBS, replace with methanol, store at -20oC.Rehydrate by slow
单克隆抗体的研究进展
单克隆抗体药物的发展起源于1975年，杂交瘤技术的问世使大量制备均一的鼠源单克隆抗体成为可能。1986年第一个抗移植后免疫排斥反应的鼠源单克隆抗体muromonab-CD3(OKT3)，经美国食品药品监督管理局（Food and Drug Administration, FDA）批准上市，[2]
单克隆抗体药物的发展起源
单克隆抗体药物的发展起源于1975年，杂交瘤技术的问世使大量制备均一的鼠源单克隆抗体成为可能。1986年第一个抗移植后免疫排斥反应的鼠源单克隆抗体muromonab-CD3(OKT3)，经美国食品药品监督管理局（Food and Drug Administration, FDA）批准上市，但是来源于
单克隆抗体的研究进展
单克隆抗体药物的发展起源于1975年，杂交瘤技术的问世使大量制备均一的鼠源单克隆抗体成为可能。1986年第一个抗移植后免疫排斥反应的鼠源单克隆抗体muromonab-CD3(OKT3)，经美国食品药品监督管理局（Food and Drug Administration, FDA）批准上市，[2]
单抗的研究进展
单克隆抗体药物的发展起源于1975年,杂交瘤技术的问世使大量制备均一的鼠源单克隆抗体成为可能。1986年第一个抗移植后免疫排斥反应的鼠源单克隆抗体muromonab-CD3(OKT3)经美国食品药品监督管理局（Food and Drug Administration, FDA）批准上市， 但是来
关于单克隆抗体的研究进展介绍
单克隆抗体药物的发展起源于1975年，杂交瘤技术的问世使大量制备均一的鼠源单克隆抗体成为可能。1986年第一个抗移植后免疫排斥反应的鼠源单克隆抗体muromonab-CD3(OKT3)，经美国食品药品监督管理局（Food and Drug Administration, FDA）批准上市，但是来
Rodent－Retinal－Ganglion－Cell－Cultures
实验概要Central neurons lose the ability for axonal regrowth during development and typically do not regenerate their axons following axotomy once the
Wes全自动蛋白质表达定量分析系统应用于微量脑组织蛋...
Wes全自动蛋白质表达定量分析系统应用于微量脑组织蛋白表达分析中脑多巴胺能神经元与帕金森、药物滥用密切相关帕金森病和药物滥用障碍都与中脑多巴胺能神经元的功能改变有关。在外侧中脑，黑质(SN)的多巴胺能神经元(SN)向背侧纹状体发出投射，参与控制运动，而位于腹侧被盖区(VTA)的多巴胺能神经元(VTA