推荐产品
生物来源
goat
质量水平
偶联物
unconjugated
抗体形式
IgG fraction of antiserum
抗体产品类型
secondary antibodies
克隆
polyclonal
表单
buffered aqueous solution
技术
indirect ELISA: 1:10,000
quantitative precipitin assay: 3.0 mg/mL
运输
dry ice
储存温度
−20°C
靶向翻译后修饰
unmodified
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一般描述
人IgG是糖蛋白抗体,含有两条相等的轻链和一对相同的重链。 IgG具有四种不同亚型,范围从IgG1到IgG4。这些抗体可调节机体对过敏和病原性感染的免疫反应。IgG还与补体结合和自身免疫疾病有关。通过免疫电泳对正常人血清和 IgG 进行测试时,抗人 IgG(全分子)抗体对人 IgG 具有特异性。该抗体还与轻链反应。免疫球蛋白G(IgG)属于免疫球蛋白家族,是一种广泛表达的血清抗体。它由γ恒定 (C) 区的重链组成。该抗体的一级结构包含连接两条重链、重链和轻链,并位于链内的二硫键。
免疫原
人 IgG
外形
溶于0.01M磷酸盐缓冲盐水,pH 7.4,含有15 mM叠氮化钠作为防腐剂
免责声明
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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储存分类代码
10 - Combustible liquids
WGK
nwg
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
常规特殊物品
历史批次信息供参考:
分析证书(COA)
Scientific reports, 8(1), 4417-4417 (2018-03-15)
Fluorodeoxyglucose (FDG) uptake by alveolar echinococcosis (AE) liver lesions is a signal of their metabolic activity and of disease progression. In order to find a surrogate marker for this status, we investigated whether parameters of the peripheral and/or periparasitic immune
eLife, 4, e08961-e08961 (2015-10-17)
DnaK/Hsp70 chaperones form oligomers of poorly understood structure and functional significance. Site-specific proteolysis and crosslinking were used to probe the architecture of oligomers formed by the endoplasmic reticulum (ER) Hsp70, BiP. These were found to consist of adjacent protomers engaging
Journal of virology, 97(2), e0189422-e0189422 (2023-02-07)
The ability of Epstein-Barr virus (EBV) to switch between latent and lytic infection is key to its long-term persistence, yet the molecular mechanisms behind this switch remain unclear. To investigate transcriptional events during the latent-to-lytic switch, we utilized Precision nuclear
Cellulose (London, England), 1-11 (2021-07-27)
Lateral flow assay (LFA) is an important point-of-care (POC) test platform due to the associated portability, on-site testing, and low cost for diagnosis of pathogen infections and disease biomarkers. However, compared to high-end analyzers in hospitals, LFA devices, in particular
Communications biology, 7(1), 842-842 (2024-07-11)
Identifying high-affinity antibodies in human serum is challenging due to extremely low number of circulating B cells specific to the desired antigens. Delays caused by a lack of information on the immunogenic proteins of viral origin hamper the development of
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