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引用和文献 (3)
Invitrogen™
AbC™ 抗大鼠/仓鼠微球试剂盒
The AbC™ Anti-Rat/Hamster Antibody Compensation Bead Kit provides a consistent, accurate, and simple-to-use technique for the setting of flow cytometry了解更多信息
| 货号 | 数量 |
|---|---|
| A10389 | 1 kit |
货号 A10389
价格（CNY)
4,198.00
飞享价
Ends: 31-Dec-2025
5,578.00共减 1,380.00 (25%)
Each
数量:
1 kit
价格（CNY)
4,198.00
飞享价
Ends: 31-Dec-2025
5,578.00共减 1,380.00 (25%)
Each
The AbC™ Anti-Rat/Hamster Antibody Compensation Bead Kit provides a consistent, accurate, and simple-to-use technique for the setting of flow cytometry compensation when using fluorochrome-conjugated to rat or hamster antibodies with any laser in flow cytometry.
• Species reactivity—for use with all isotypes of rat and hamster antibody conjugates
• Maximum laser compatibility—for use with all lasers
Accurate compensation is crucial for effective multicolor analysis in flow cytometry. Often, however, cellular-based compensation controls are not completely effective, as many antigens are not highly expressed, and dimly stained cells can lead to inaccurate compensation settings. The AbC™ Anti-Rat/Hamster Bead Kit was developed to address this issue.
View a selection guide for all flow cytometry compensation beads.
How it works
Each kit provides polystyrene microspheres that have fluorescent antibody conjugate capture capacity (positive compensation beads) or are inert (negative compensation beads). After mixing with a fluorophore-conjugated rat or hamster antibody, the two components provide a distinct high-signal positive control with an appropriate negative population that can then be used to set compensation properly regardless of the intensity of the cells in the actual experiment.
Species reactivity
The AbC™ Anti-Rat/Hamster Bead Kit is ideal for compensation with all isotypes of rat (IgG1, IgG2a, IgG2b, IgG2c, IgM) and hamster (Armenian IgG and Syrian IgG) immunoglobulins.
Maximum laser compatibility
All AbC™ Compensation Bead Kits are ideal for use with any excitation source, including the 405 nm laser which has historically provided higher background signals due to auto-fluorescence with other kits on the market.
• Species reactivity—for use with all isotypes of rat and hamster antibody conjugates
• Maximum laser compatibility—for use with all lasers
Accurate compensation is crucial for effective multicolor analysis in flow cytometry. Often, however, cellular-based compensation controls are not completely effective, as many antigens are not highly expressed, and dimly stained cells can lead to inaccurate compensation settings. The AbC™ Anti-Rat/Hamster Bead Kit was developed to address this issue.
View a selection guide for all flow cytometry compensation beads.
How it works
Each kit provides polystyrene microspheres that have fluorescent antibody conjugate capture capacity (positive compensation beads) or are inert (negative compensation beads). After mixing with a fluorophore-conjugated rat or hamster antibody, the two components provide a distinct high-signal positive control with an appropriate negative population that can then be used to set compensation properly regardless of the intensity of the cells in the actual experiment.
Species reactivity
The AbC™ Anti-Rat/Hamster Bead Kit is ideal for compensation with all isotypes of rat (IgG1, IgG2a, IgG2b, IgG2c, IgM) and hamster (Armenian IgG and Syrian IgG) immunoglobulins.
Maximum laser compatibility
All AbC™ Compensation Bead Kits are ideal for use with any excitation source, including the 405 nm laser which has historically provided higher background signals due to auto-fluorescence with other kits on the market.
仅供科研使用。不可用于诊断程序。
规格
检测方法荧光
直径（公制）6 μm
发射任意激光（UV 至 633/635）
适用于（设备）流式细胞仪
产品规格管装
数量1 kit
运输条件室温
染色剂配置表面
产品线CompenFlow、Molecular Probes
产品类型补偿微珠
Unit SizeEach
内容与储存
包含 1 瓶 AbC™ 抗大鼠/仓鼠捕获微珠和 1 瓶阴性微珠。储存于 2°C 至 8°C
常见问题解答 (FAQ)
我在进行流式细胞实验时，补偿值超过100，可能出现这种情况吗？
有人告诉我说我需要补偿自己的流式细胞分析数据，这是什么意思？
流式细胞分析该选用哪种类型的对照？
在流式细胞分析中为何要担心补偿？
如何为抗体设置补偿对照？
引用和文献 (3)
引用和文献
Abstract
Identification and characterization of intestinal antigen-presenting cells involved in uptake and processing of a nontoxic recombinant chimeric mucosal immunogen based on cholera toxin using imaging flow cytometry.
Journal:
PubMed ID:24197893
'Intragastric immunization with recombinant chimeric immunogen, SBR-CTA2/B, constructed from the saliva-binding region (SBR) of Streptococcus mutans antigen AgI/II and the A2/B subunits of cholera toxin (CT) induces salivary and circulating antibodies against S. mutans that protect against dental caries. We previously found that SBR-CTA2/B activated dendritic cells (DC) in the
Multiparametric analysis of host response to murine cytomegalovirus in MHC class I-disparate mice reveals primacy of Dk-licensed Ly49G2+ NK cells in viral control.
Journal:
PubMed ID:24068668
MHC class I D(k) and Ly49G2 (G2) inhibitory receptor-expressing NK cells are essential to murine CMV (MCMV) resistance in MA/My mice. Without D(k), G2(+) NK cells in C57L mice fail to protect against MCMV infection. As a cognate ligand of G2, D(k) licenses G2(+) NK cells for effector activity. These
Self MHC class I-licensed NK cells enhance adaptive CD8 T-cell viral immunity.
Journal:Blood
PubMed ID:21436069
MHC class I (MHC I) is essential to NK- and T-cell effector and surveillance functions. However, it is unknown whether MHC I polymorphism influences adaptive immunity through NK cells. Previously, we found that MHC I D(k), a cognate ligand for the Ly49G2 inhibitory receptor, was essential to NK control of