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特异性
This product was prepared from monospecific antiserum by immunoaffinity chromatography using Human antigens coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities, pepsin digestion and chromatographic separation. Assay by immunoelectrophoresis resulted in a single precipitin arc against Human IgA, Anti-Peroxidase and Anti-Goat Serum. No reaction was observed against Anti-Pepsin or Anti-Goat IgG F(c). Specificity was confirmed by ELISA at less than 1% cross reactivity against other Human heavy or light chain isotypes.
免疫原
Human IgA alpha heavy chain
物理属性
Antibody format: IgG F(ab′)2
外形
Supplied in 0.01 M Sodium Phosphate, 0.25 M Sodium Chloride, pH 7.2 with 15 mg/mL Bovine Serum Albumin (BSA) - Immunoglobulin and Protease free
重悬
Reconstitute with 500 μ;L deionized water (or equivalent).
免责声明
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.
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储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
其他客户在看
Marne Azarias Da Silva et al.
Science advances, 9(31), eadg2122-eadg2122 (2023-08-04)
Since the initial spread of severe acute respiratory syndrome coronavirus 2 infection, several viral variants have emerged and represent a major challenge for immune control, particularly in the context of vaccination. We evaluated the quantity, quality, and persistence of immunoglobulin
André Santa Cruz et al.
Nature communications, 14(1), 1772-1772 (2023-03-31)
Several millions of individuals are estimated to develop post-acute sequelae SARS-CoV-2 condition (PASC) that persists for months after infection. Here we evaluate the immune response in convalescent individuals with PASC compared to convalescent asymptomatic and uninfected participants, six months following
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