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BD Pharmingen™ APC Mouse IgG1 κ Isotype Control
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BD Pharmingen™ APC Mouse IgG1 κ Isotype Control

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品牌: BD Pharmingen
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实验应用:
Intracellular staining (flow cytometry), Isotype control (Routinely Tested)
产品介绍
产品介绍
产品信息
荧光素标记
简单描述
The MOPC-21 immunoglobulin is a mouse myeloma protein. The MOPC-21 immunoglobulin was selected as an isotype control following screening for low background on a variety of mouse and human tissues.
商品描述
MOPC-21 The MOPC-21 immunoglobulin is a mouse myeloma protein. The MOPC-21 immunoglobulin was selected as an isotype control following screening for low background on a variety of mouse and human tissues.
同种型
Mouse IgG1, κ
克隆号
克隆 MOPC-21 (RUO)
浓度
0.2 mg/ml
产品详情
APC
Allophycocyanin (APC), is part of the BD family of phycobiliprotein dyes. This fluorochrome is a multimeric fluorescent phycobiliprotein with excitation maximum (Ex Max) of 651 nm and an emission maximum (Em Max) at 660 nm. APC is designed to be excited by the Red (627-640 nm) laser and detected using an optical filter centered near 660 nm (e.g., a 660/20 nm bandpass filter). Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
APC
Red 627-640 nm
651 nm
660 nm
应用
实验应用
Intracellular staining (flow cytometry), Isotype control (Routinely Tested)
目标/特异性
IgG1 kappa
制备和贮存
存储溶液
Aqueous buffered solution containing ≤0.09% sodium azide.
文献
文献
研发参考(1) 1. Prussin C, Metcalfe DD. Detection of intracytoplasmic cytokine using flow cytometry and directly conjugated anti-cytokine antibodies. J Immunol Methods. 1995; 188(1):117-128. (Methodology).

参考图片

Expression of TNF by stimulated human peripheral blood mononuclear cells (PBMC). Human PBMC were stimulated for 6 hours with PMA (50 ng/ml final concentration; Sigma) and calcium ionophore A23187 (1 µg/ml final concentration; Sigma), in the presence of GolgiStop™ (2 µM final concentration; Cat. No. 554724). The PMBC were stained with FITC-anti-CD3 (FITC-UCHT1, Cat. No. 555332), fixed, permeabilized, and subsequently stained with 0.125 µg of APC-mouse anti-human TNF (APC-MAb11, Cat. No. 554514, left panel) or with 0.125 µg APC-mouse IgG1 (Cat. No. 554681, right panel) using BD Pharmingen™ staining protocol. To demonstrate specificity, the binding of APC-MAb11 antibody was blocked by perincubation of fixed/permabilized cells with excess unlabelled MAb11 antibody (5 µg; Cat. No. 554510). The quadrant markers for the bivariate dot plot were set based on isotype controls and verified using the unlabelled MAb11 antibody blocking control. The APC-conjugated reagent can be used in any flow cytometer equipped with a dye, HeNE or red diode laser. These include the dual laser FACStarPLUS™, FACSVantage™, or FACSCalibur™.

Expression of TNF by stimulated human peripheral blood mononuclear cells (PBMC). Human PBMC were stimulated for 6 hours with PMA (50 ng/ml final concentration; Sigma) and calcium ionophore A23187 (1 µg/ml final concentration; Sigma), in the presence of GolgiStop™ (2 µM final concentration; Cat. No. 554724). The PMBC were stained with FITC-anti-CD3 (FITC-UCHT1, Cat. No. 555332), fixed, permeabilized, and subsequently stained with 0.125 µg of APC-mouse anti-human TNF (APC-MAb11, Cat. No. 554514, left panel) or with 0.125 µg APC-mouse IgG1 (Cat. No. 554681, right panel) using BD Pharmingen™ staining protocol. To demonstrate specificity, the binding of APC-MAb11 antibody was blocked by perincubation of fixed/permabilized cells with excess unlabelled MAb11 antibody (5 µg; Cat. No. 554510). The quadrant markers for the bivariate dot plot were set based on isotype controls and verified using the unlabelled MAb11 antibody blocking control. The APC-conjugated reagent can be used in any flow cytometer equipped with a dye, HeNE or red diode laser. These include the dual laser FACStarPLUS™, FACSVantage™, or FACSCalibur™.

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货号:
554681
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100ug
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