推薦產品
一般說明
Immunoaffinity purified goat polyclonal antibody conjugated to alkaline phosphatase. Recognizes human IgG γ-chain.
This Goat Anti-Human IgG, γ-Chain Specific Alk-Phos Conjugate is validated for use in Enzyme Immunoassay, Immunoelectrophoresis for the detection of Human IgG, γ-Chain Specific.
免疫原
Human
應用
Enzyme Immunoassay (1:5000)
Immunoelectrophoresis (see comments)
Immunoelectrophoresis (see comments)
包裝
Please refer to vial label for lot-specific concentration.
警告
Toxicity: Standard Handling (A)
外觀
In 50 mM Tris-HCl, 1 mM MgCl₂, 0.1 mM ZnCl₂, 1% BSA, pH 8.0.
其他說明
Monospecific for human IgG γ-chain as determined by immunoelectrophoresis against normal human serum. p-Nitrophenylphosphate, 1 mg/ml in 10% diethanolamine, pH 9.8, 1 mM MgCl2 at 25°C, was used as substrate for testing immunoenzyme reactivity. Variables associated with assay conditions will dictate the proper working dilution.
法律資訊
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
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儲存類別代碼
12 - Non Combustible Liquids
水污染物質分類（WGK）
WGK 2
閃點（°F）
Not applicable
閃點（°C）
Not applicable
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號，寫有 ‘Lot’或‘Batch’.。
Pauline Versteegen et al.
Frontiers in immunology, 13, 864674-864674 (2022-06-10)
Immunogenicity of acellular pertussis (aP) vaccines is conventionally assessed by measuring antibody responses but antibody concentrations wane quickly after vaccination. Memory B cells, however, are critical in sustaining long-term protection and therefore may be an important factor when assessing pertussis
Malick M Gibani et al.
Nature medicine, 25(7), 1082-1088 (2019-07-05)
Salmonella Typhi is a human host-restricted pathogen that is responsible for typhoid fever in approximately 10.9 million people annually1. The typhoid toxin is postulated to have a central role in disease pathogenesis, the establishment of chronic infection and human host
Angela M Minassian et al.
Med (New York, N.Y.), 2(6), 701-719 (2021-07-06)
Development of an effective vaccine against the pathogenic blood-stage infection of human malaria has proved challenging, and no candidate vaccine has affected blood-stage parasitemia following controlled human malaria infection (CHMI) with blood-stage Plasmodium falciparum. We undertook a phase I/IIa clinical
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