APC Mouse IgG1 κ Isotype Control

BD Pharmingen™ APC Mouse IgG1 κ Isotype Control

Name: APC Mouse IgG1 κ Isotype Control
Brand: BD Pharmingen™
SKU: 554681

クローン MOPC-21

(RUO)

すべてのフォーマットを表示

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Scientific Resources

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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製品詳細

Brand: BD Pharmingen™

Isotype: Mouse IgG1, κ

Application: Intracellular staining (flow cytometry), Isotype control (Routinely Tested)

Concentration: 0.2 mg/ml

RRID: AB_398576

Storage Buffer: Aqueous buffered solution containing ≤0.09% sodium azide.

Regulatory Status: RUO

Preparation and Storage

The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. The antibody was conjugated to APC under optimum conditions, and unconjugated antibody and free APC were removed. Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze.

推奨アッセイ手順

Immunofluorescent Staining and Flow Cytometric Analysis: The APC-MOPC-21 immunoglobulin (Cat. No. 554681) is a suitable mouse IgG1 isotype control for assessing the level of background staining on paraformaldehyde fixed/saponin-permeabilized mouse or human cells for flow cytometric analysis. Use at comparable concentrations to antibody of interest (e.g., ≤ 0.5 µg mAb/1 million cells) (see figure). For specific methodology, visit the protocols section of our website, or refer to the Immune Function Handbook, which is posted on our web site at www.bdbiosciences.com

Product Notices

Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
Since applications vary, each investigator should titrate the reagent to obtain optimal results.
For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
This APC-conjugated reagent can be used in any flow cytometer equipped with a dye, HeNe, or red diode laser.
Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.

554681 Rev. 3

抗体の詳細

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.

554681 Rev. 3

フォーマットの詳細

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.

フォーマット: APC

励起源: Red 627-640 nm

最大励起波長: 651 nm

最大蛍光波長: 660 nm

554681 Rev.3

引用＆参考文献

Development References (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). View Reference

554681 Rev. 3

Please refer to Support Documents for Quality Certificates

Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described

Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.

For Research Use Only. Not for use in diagnostic or therapeutic procedures.