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Merck
CN
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主要文件

401132

Sigma-Aldrich

Goat Anti-Human IgA, α-Chain Specific Alkaline Phosphatase Conjugate

liquid, Calbiochem®

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About This Item

UNSPSC代码:
12352203
NACRES:
NA.74

生物来源

goat

质量水平

抗体形式

affinity isolated antibody

抗体产品类型

secondary antibodies

克隆

polyclonal

表单

liquid

包含

≤0.1% sodium azide as preservative

制造商/商品名称

Calbiochem®

储存条件

do not freeze

同位素/亚型

IgG

运输

wet ice

储存温度

2-8°C

一般描述

Immunoaffinity purified goat polyclonal antibody, conjugated to alkaline phosphatase. Recognizes human IgA, α-chain.
This Goat Anti-Human IgA, α-Chain Specific Alk-Phos Conjugate is validated for use in Enzyme Immunoassay, Immunoelectrophoresis for the detection of Human IgA, α-Chain Specific.

包装

Please refer to vial label for lot-specific concentration.

警告

Toxicity: Standard Handling (A)

外形

In 50 mM Tris, 1 mM MgCl₂, 0.1 mM ZnCl₂, 1% BSA, pH 7.6.

其他说明

p-Nitrophenyl phosphate, 1.0 mg/ml in 10% diethanolamine, pH 9.8, 1 mM MgCl2 at 25°C, was used as substrate for testing immunoenzyme reactivity. Monospecific for human immunoglobulin A, α-chain as determined by immunoelectrophoresis against normal human serum. Variables associated with assay conditions will dictate the proper working dilution.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

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储存分类代码

12 - Non Combustible Liquids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Primary immunization of infants with protein-polysaccharide conjugate vaccines induces antipolysaccharide antibody and is highly effective in preventing invasive disease caused by encapsulated bacteria. However, recent experience from the UK indicates that this immunity is not sustained in the absence of
Malick M Gibani et al.
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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
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A growing number of studies indicate that coronavirus disease 2019 (COVID-19) is associated with inflammatory sequelae, but molecular signatures governing the normal versus pathologic convalescence process have not been well-delineated. Here, we characterized global immune and proteome responses in matched

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