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Merck
CN

P9670

抗 小鼠 IgG(全分子)-R-藻红蛋白 山羊抗

affinity isolated antibody, buffered aqueous solution

别名:

GoatAnti-Mouse IgG (whole molecule)–R-PE

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.46
MDL number:
Conjugate:
phycoerythrin (R-PE) conjugate
Clone:
polyclonal
Application:
indirect immunofluorescence
Technique(s):
indirect immunofluorescence: 1:20
Citations:
17
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产品名称

抗 小鼠 IgG(全分子)-R-藻红蛋白 山羊抗, affinity isolated antibody, buffered aqueous solution

biological source

goat

conjugate

phycoerythrin (R-PE) conjugate

antibody form

affinity isolated antibody

antibody product type

secondary antibodies

clone

polyclonal

form

buffered aqueous solution

technique(s)

indirect immunofluorescence: 1:20

shipped in

wet ice

storage temp.

2-8°C

target post-translational modification

unmodified

Quality Level

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Application

Anti-mouse IgG (whole molecule)-R-phycoerythrin antibody can be used as secondary antibody in immunocytofluorimetric analysis. It can also be used in immunohistochemistry and indirect immunofluorescence.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

General description

IgG is the main antibody type found in plasma and extracellular fluid and is expressed on B cell membrane. It plays a pivotal role in humoral immune responses like phagocytosis and complement activation.Anti-mouse IgG (whole molecule)-R-phycoerythrin antibody (diluted 1: 20) can be used as secondary antibody in fluorescence-activated cell sorting (FACS) analysis. It can also be used in flow cytometry. Goat anti-mouse IgG (whole molecule)-R-phycoerythrin antibody reacts specifically with mouse IgG and its subclasses IgG1, IgG2a, IgG2b, and IgG3. This product has also shown reactivity for mouse IgA and IgM but does not react with human serum proteins.

Immunogen

Purified mouse IgG.

Other Notes

Antibody adsorbed with human serum proteins.

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 0.1 mM EDTA, 1 mM iodoacetamide,
1% bovine serum albumin and 15 mM sodium azide.

Preparation Note

Adsorbed to reduce background with human samples.

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存储类别

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

常规特殊物品
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分析证书(COA)

Lot/Batch Number

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Juliane Medler et al.
Cell death & disease, 10(3), 224-224 (2019-03-06)
Antibodies specific for TNFRSF receptors that bind soluble ligands without getting properly activated generally act as strong agonists upon FcγR binding. Systematic analyses revealed that the FcγR dependency of such antibodies to act as potent agonists is largely independent from
Michael Heyne et al.
Nature communications, 11(1), 297-297 (2020-01-17)
Quantifying the effects of various mutations on binding free energy is crucial for understanding the evolution of protein-protein interactions and would greatly facilitate protein engineering studies. Yet, measuring changes in binding free energy (ΔΔGbind) remains a tedious task that requires
Paul L Bollyky et al.
Journal of immunology (Baltimore, Md. : 1950), 179(2), 744-747 (2007-07-10)
Hyaluronan is a glycosaminoglycan present in the extracellular matrix. When hyaluronan is degraded during infection and injury, low m.w. forms are generated whose interactions influence inflammation and angiogenesis. Intact high m.w. hyaluronan, conversely, conveys anti-inflammatory signals. We demonstrate that high
Ira Bergman et al.
International journal of cancer, 121(2), 425-430 (2007-03-14)
Vesicular stomatitis virus (VSV) is being developed for cancer therapy. We have created a recombinant replicating VSV (rrVSV) that targeted to Her2/neu expressing breast cancer cells and expresses mouse GM-CSF. We now tested the efficacy of this rrVSV in the
Juliane Kums et al.
mAbs, 9(3), 506-520 (2017-01-18)
Cell surface antigen-specific antibodies are of substantial diagnostic and therapeutic importance. The binding properties of such antibodies are usually evaluated by cell-free assays, in particular surface plasmon resonance (SPR) analysis, or flow cytometry. SPR analyses allow the detailed quantitative and

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