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- 文献和实验
- 技术资料
- 供应商:
BD Pharmingen
- 靶点:
IgM
- 级别:
RUO
- 克隆性:
单克隆
- 抗原来源:
Human
- 抗体英文名:
IgM Antibody
- 抗体名:
IgM
- 标记物:
BUV395
- 宿主:
Mouse
- 适应物种:
Human
- 亚型:
Mouse IgG1, κ
- 形态:
液体
- 应用范围:
Flow Cytometry (FCM)
- 保存条件:
2-8℃避光保存
- 规格:
50Tests
产品概述
Hu IgM BUV395 G20-127 50Tst 为 BD Pharmingen 品牌流式抗体,货号 563903,靶向 IgM,荧光标记 BUV395,克隆 G20-127 (RUO),规格 50Tests。适用于 Flow cytometry (Routinely Tested) 检测,仅供科研使用(RUO)。
靶点与抗体说明
IgM is an important component in the first line of defense against foreign pathogens, but may also play a role in autoimmune diseases. IgM monomers consist of two light and two heavy chains. Unlike the heavy chain of an IgG antibody which contains 3 constant Ig domains, the µ heavy chain of IgM contains 4 constant Ig domains. Five IgM monomers complex with a small polypeptide (J-chain) to form pentameric IgM that can be found in human plasma. In an immune response, the binding of IgM to a cell surface antigen enables C1q to activate interactions with downstream components in the classical complement pathway. Mature B lymphocytes express IgM. The G20-127 monoclonal antibody binds to the heavy chain of human IgM. The G20-127 antibody is not thought to react with other immunoglobulin heavy chain isotypes. The antibody was conjugated to BD Horizon™ BUV395 which has been exclusively developed by BD Biosciences as an optimal dye for use on a 355 nm laser equipped instrument. With an Ex Max at 348 nm and an Em Max at 395 nm, this dye has virtually no spillover into any other detector. BD Horizon™ BUV395 can be excited with a 355 nm laser and detected with a 379/28 filter.
核心参数
| 货号 | 563903 |
| 品牌 | BD Pharmingen |
| 克隆号 | 克隆 G20-127 (RUO) |
| 宿主 | Mouse |
| 同种型 | Mouse IgG1, κ |
| 荧光标记 | BUV395 |
| 抗原 / 靶点 | IgM |
| 反应种属 | Human |
| 验证应用 | Flow cytometry (Routinely Tested) |
| 推荐用量 | 5 µl |
| 规格 | 50Tests |
| 存储缓冲液 | Aqueous buffered solution containing BSA and ≤0.09% sodium azide. |
荧光染料信息
BUV395 The BD Horizon Brilliant™ Ultraviolet 395 (BUV395) Dye is part of the BD Horizon Brilliant™ Ultraviolet family of dyes. This base dye is a polymer fluorochrome with an excitation maximum (Ex Max) of 348-nm and an emission maximum (Em Max) at 395-nm. Driven by BD innovation, BUV395 is designed to be excited by the ultraviolet laser (355-nm) and detected using an optical filter centered near 380-nm (e.g., 379/28-nm bandpass filter). BUV395 is the ideal dye when using only one detector on the ultraviolet laser as it spills into no other detectors and no other fluors spill into it. Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye. 格式:BUV395最多激发源:348 nm最多发射源:395 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 and ≤0.09% sodium azide.
参考文献
Chtanova T, Tangye SG, Newton R, et al. T follicular helper cells express a distinctive transcriptional profile, reflecting their role as non-Th1/Th2 effector cells that provide help for B cells. J Immunol. 2004; 173(1):68-78. (Clone-specific: Flow cytometry). Le Gallou S, Caron G, Delaloy C, Rossille D, Tarte K, Fest T. IL-2 requirement for human plasma cell generation: coupling differentiation and proliferation by enhancing MAPK-ERK signaling. J Immunol. 2012; 189(1):161-173. (Clone-specific: Flow cytometry). Mei HE, Yoshida T, Sime W, et al. Blood-borne human plasma cells in steady state are derived from mucosal immune responses. Blood. 2009; 113(11):2461-2469. (Clone-specific: Flow cytometry, Immunofluorescence). Widhopf GF, 2nd, Brinson DC, Kipps TJ, Tighe H. Transgenic expression of a human polyreactive Ig expressed in chronic lymphocytic leukemia generates memory-type B cells that respond to nonspecific immune activation. J Immunol. 2004; 172(4):2092-2099. (Clone-specific: Flow cytometry). Zola H, Macardle PJ, Flego L, Webster J. The expression of sub-population markers on B cells: a re-evaluation using high-sensitivity fluorescence flow cytometry. Dis Markers. 1991; 9(2):103-118. (Biology: Cell differentiation, Dot Blot, Flow cytometry, Fluorescence activated cell sorting, In situ hybridization).
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文献和实验ul ,混匀;混匀后从第五、第六孔中各取 50 μ l分别加到第七、第八孔中,再在第七、第八孔中分别加标准品稀释液 50 μ l,混匀后从第七、第八孔中分别取 50 μ l加到第九、第十孔中,再在第九第十孔分别加标准品稀释液 50 μ l,混匀后从第九第十孔中各取 50 μ l弃掉。(稀释后各孔加样量都为 50 μ l,浓度分别为 60 μ g/ml ,40 μ g/ml ,20 μ g/ml ,10 μ g/ml ,5 μ g/ml)。 2. 加样:分别设空白孔(空白
实验。若不能马上进行试验,可 将标本放于 -20 ℃保存,但 应 避免反复冻融 . 7. 不能检测含NaN3的样品 ,因NaN3 抑制辣根过氧化物酶的( HRP )活性。 操作步骤 1. 标准品的稀释与加样:在酶标包被板上设标准品孔10 孔,在第一、第二孔中分别加标准品 100 μ l,然后在第一、第二孔中加标准品稀释液 50 μ l,混匀;然后从第一孔、第二孔中各取 100 μ l分别加到第三孔和第四孔,再在第三、第四孔分别加标准品稀释液 50 μ l
g离心20min,可见辛酸因温度低而从系统中结晶析出漂浮在腹水上层,弃去此结晶以及底部沉淀,向上清中加入1/10体积的10×PBS(0.1M,pH 7.4),4 ℃条件下向其中加入硫酸铵固体至终浓度为0.277 g/ml,静置1h以上; (3)10000 g离心20min;弃上清,将沉淀溶于适量PBS中,再将其装入透析袋对PBS透析(透析液应为抗体体积的100倍以上,最好搅拌),4 ℃过夜; (4)收集透析好的抗体,直接现用或加入保护剂和防腐剂长期保存。保存条件同多抗保存
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