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Key Documents

M0659

Sigma-Aldrich

抗-小鼠IgG (Fab特异性) F(ab′)2片段 山羊抗

affinity isolated antibody

同義詞:

Anti-Mouse Fab Fragment, Fab Specific Detection, Goat Anti-Mouse IgG Fab

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About This Item

MDL號碼:
分類程式碼代碼:
12352203
NACRES:
NA.46

生物源

goat

品質等級

共軛

unconjugated

抗體表格

affinity isolated antibody

抗體產品種類

secondary antibodies

無性繁殖

polyclonal

濃度

2.0 mg/mL

技術

indirect ELISA: suitable

運輸包裝

dry ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

一般說明

免疫球蛋白G(IgG)是一种糖蛋白抗体,可调节免疫反应(如吞噬作用),也可影响自身免疫疾病的进程。小鼠IgG具有四种不同的同种型,即IgG1、IgG2a、IgG2b和IgG3。IgG1调节小鼠中的补体结合
抗小鼠IgG(Fab特异性)F(ab′)2片段抗体是单特异性的,通过免疫电泳相对于正常小鼠血清、小鼠IgG和小鼠IgG的Fab片段所确定的。该抗体不与小鼠IgG的Fc片段反应。此外,通过ELISA测定,未观察到与人κ或λ轻链、IgG、IgA、IgM、IgD和IgE、牛IgG和IgM或马IgG的反应性。在免疫电泳中,发现抗体制剂仅由山羊IgG的F(ab′)2片段组成,其中将特异性抗血清应用于山羊IgG片段。未观察到山羊IgG全分子污染。

免疫原

小鼠IgG

應用

抗小鼠IgG(Fab特异性)F(ab′)2片段抗体适用于ELISA(使用浓度为2μg/mI(100 μg/孔)的50 mM碳酸盐/碳酸氢盐缓冲液,pH9.6)。该抗体也可用于免疫电泳。

其他說明

经过牛、马和人血清蛋白吸附的抗体。

外觀

0.01M 磷酸缓冲盐溶液,pH 7.4,含 15mM 叠氮化钠。

免責聲明

除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。

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儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

nwg

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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T E Steinsvik et al.
Scandinavian journal of immunology, 42(6), 607-616 (1995-12-01)
SCID and RAG-2 deficient mice were transplanted intraperitoneally with human peripheral blood lymphocytes (hu-PBL-SCID and hu-PBL-RAG mice). Seven days after transplantation the mice were immunized with a pneumococcal polysaccharide vaccine. Flow cytometry analysis of cells from the peritoneal cavity and
The Ocular Conjunctiva as a Mucosal Immunization Route: A Profile of the Immune Response to the Model Antigen Tetanus Toxoid
Barisani-Asenbauer T, et al.
PLoS ONE, 8(4) (2013)
Peter Engelhardt et al.
Methods in molecular biology (Clifton, N.J.), 369, 387-405 (2007-07-28)
Standard immunogold-labeling methods in transmission electron microscopy (TEM) are unable to locate immunogold particles in the depth direction. This inability does not only concern bulky whole mounts, but also sections. A partial solution to the problem is stereo inspection. However
J Wang et al.
Journal of neuroscience research, 50(1), 23-31 (1997-10-23)
The role of the transcription factor AP-1 in regulating D2 receptor transcriptional activity was investigated in D2 receptor expressing neuroblastoma cells, NB41A3, and in non-D2 receptor expressing CHO cells. Deletion of a region containing the putative AP-1 binding site resulted
Chen Yang et al.
Molecular medicine reports, 18(2), 1353-1360 (2018-06-15)
Previous studies have demonstrated that lipid rafts and β‑adducin serve an important role in leukocyte rolling. In the present study the migratory ability and behavior of neutrophils was demonstrated to rely on the integrity of the lipid raft structure. β‑adducin

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