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- 详细信息
- 文献和实验
- 技术资料
- 库存:
999
- 供应商:
biorbyt
- 检测范围:
46.88-3000pg/mL
- 检测方法:
Sandwich
- 适应物种:
Human
- 样本:
serum, plasma, Tissue homogenate and Other biological samples
- 灵敏度:
28.13 pg/mL
- 规格:
48 T
产品别名:FcγRⅡ, CD32
应用笔记:This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human FcγR Ⅱ/CD32. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Human FcγR Ⅱ/CD32 and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Human FcγR Ⅱ/CD32, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Human FcγR Ⅱ/CD32. You can calculate the concentration of Human FcγR Ⅱ/CD32 in the samples by comparing the OD of the samples to the standard curve.
实验时长:3.5H
UniProt ID:P31994
靶点:FcγRⅡ/CD32
Note:For research use only.
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文献和实验载体 8.淋巴因子 9.过继免疫 10.主要组织相容性复合体 三、选择题(每小题4分,共20分) 1.Ⅱ类HLA抗原在以下哪种细胞膜上不能检出: A、静止T细胞 B、单核细胞 C、B细胞 D、激活T细胞 2.用胃蛋白酶可将IgG分子水介成: A、Fab’ B、F(ab’)2 C、F(ab’)2+Fc D、2Fab+Fc 3.下列哪种物质免疫原性最弱: A、多糖 B、蛋白质 C、脂 D、核酸 4.下列哪一个是中枢淋巴器官: A、扁桃体 B
[资源] 所有的看家基因(housekeeping genes)列表+引物设计服务
_021642 Homo sapiens Fc fragment of IgG, low affinity IIa, receptor for (CD32) (FCGR2A), mRNA 772 NM_005354 Homo sapiens jun D proto-oncogene (JUND), mRNA 4967 NM_020529 Homo sapiens nuclear factor of kappa light polypeptide gene enhancer in B
;170:827 5.Lanier LL ,et al. Co-association of CD3ζ with a receptor (CD16)for IgG Fc on human natural killer cells.Nature,1989;342:803 6.Miller JFAP. The role of the thymus in immunity. Thirty years of progress. The Immunologist,1993;(1):9







