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- 技术资料
- 供应商:
BD Pharmingen
- 靶点:
TCR β Chain
- 级别:
RUO
- 克隆性:
单克隆
- 抗原来源:
Mouse
- 抗体英文名:
TCR β Chain Antibody
- 抗体名:
TCR β Chain
- 标记物:
PE-CF594
- 宿主:
Armenian
- 适应物种:
Mouse
- 免疫原:
TCR affinity-purified from mouse T-cell hybridoma DO-11.10
- 亚型:
Armenian Hamster IgG2, λ1
- 形态:
液体
- 应用范围:
Flow Cytometry (FCM)
- 保存条件:
2-8℃避光保存
- 规格:
50 ug
产品概述
Ms TCR Bta Chain PE-CF594 H57-597 50ug 为 BD Pharmingen 品牌流式抗体,货号 562841,靶向 TCR β Chain,荧光标记 PE-CF594,克隆 H57-597 (RUO),规格 50 ug。适用于 Flow cytometry (Routinely Tested) 检测,仅供科研使用(RUO)。
靶点与抗体说明
The H57-597 antibody reacts with a common epitope of the β chain of the T-cell Receptor (TCR) complex on αβ TCR-expressing thymocytes, peripheral T lymphocytes, NK1.1+ thymocytes, and NK-T cells of all mouse strains tested. It does not react with γδ TCR-bearing T cells. In the fetal and adult thymus, the TCR β-chain may form homodimers or pair with the pre-TCR α-chain on the surface of immature thymocytes before TCR α-chain expression. Plate-bound or soluble H57-597 antibody activates αβ TCR-bearing T cells, and plate-bound mAb can induce apoptotic death. This antibody is conjugated to BD Horizon™ PE-CF594, which has been developed exclusively by BD Biosciences as a better alternative to PE-Texas Red®. PE-CF594 excites and emits at similar wavelengths to PE-Texas Red® yet exhibits improved brightness and spectral characteristics. Due to PE having maximal absorption peaks at 496 nm and 564 nm, PE-CF594 can be excited by the blue (488-nm), green (532-nm) and yellow-green (561-nm) lasers and can be detected with the same filter set as PE-Texas Red® (eg 610/20-nm filter).
核心参数
| 货号 | 562841 |
| 品牌 | BD Pharmingen |
| 克隆号 | 克隆 H57-597 (RUO) |
| 宿主 | Armenian |
| 同种型 | Armenian Hamster IgG2, λ1 |
| 荧光标记 | PE-CF594 |
| 抗原 / 靶点 | TCR β Chain |
| 反应种属 | Mouse |
| 验证应用 | Flow cytometry (Routinely Tested) |
| 免疫原 | TCR affinity-purified from mouse T-cell hybridoma DO-11.10 |
| 规格 | 50 ug |
| 存储缓冲液 | Aqueous buffered solution containing BSA, protein stabilizer, and ≤0.09% sodium azide. |
荧光染料信息
PE-CF594 BD Horizon™ PE-CF594 dye is a part of the BD PE family of dyes. This tandem fluorochrome is comprised of a R-Phycoerythrin (PE) donor that has excitation maxima (Ex Max) of 496-nm and 566-nm and an acceptor dye with an emission maximum (Em Max) at 615-nm. PE-CF594, driven by BD innovation, is designed to be excited by the blue (488-nm), Green (532-nm) and yellow-green (561-nm) lasers and detected using an optical filter centered near 615 nm (e.g., a 610/20-nm bandpass filter). The donor dye can be excited by the Blue (488-nm), Green (532-nm) and yellow-green (561-nm) lasers and the acceptor dye can be excited by the green (532-nm) laser resulting in cross-laser excitation and fluorescence spillover. Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye. 格式:PE-CF594最多激发源:496 nm, 566 nm最多发射源:615 nm
保存与运输
建议 2-8℃ 避光保存,请勿冷冻,避免反复冻融。 存储缓冲液:Aqueous buffered solution containing BSA, protein stabilizer, and ≤0.09% sodium azide.
参考文献
Castro JE, Listman JA, Jacobson BA, et al. Fas modulation of apoptosis during negative selection of thymocytes. Immunity. 1996; 5(6):617-627. (Clone-specific: Flow cytometry, Fluorescence microscopy, Immunofluorescence). Gascoigne NR. Transport and secretion of truncated T cell receptor beta-chain occurs in the absence of association with CD3. J Biol Chem. 1990; 265(16):9296-9301. (Clone-specific: Immunofluorescence, Immunoprecipitation). Kruisbeek AM, Shevach EM. Proliferative assays for T cell function. Curr Protoc Immunol. 2004; 3:3.12.1-3.12.14. (Clone-specific: Activation, Functional assay, Stimulation). Kubo RT, Born W, Kappler JW, Marrack P, Pigeon M. Characterization of a monoclonal antibody which detects all murine alpha beta T cell receptors. J Immunol. 1989; 142(8):2736-2742. (Immunogen: Activation, Flow cytometry, Functional assay, Stimulation). Saint-Ruf C, Panigada M, Azogui O, Debey P, von Boehmer H, Grassi F. Different initiation of pre-TCR and gammadeltaTCR signalling. Nature. 2000; 406(6795):524-527. (Clone-specific: Flow cytometry, Fluorescence microscopy, Immunofluorescence, Immunoprecipitation, Western blot).
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