Native 人Serum Albumin蛋白(ab205808)
Key features and details
- Expression system: Native
- Purity: > 95% SDS-PAGE
- Suitable for: SDS-PAGE
描述
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产品名称
Native 人Serum Albumin蛋白
参阅全部 Human Serum Albumin 蛋白酶 -
纯度
> 95 % SDS-PAGE.
Purified from normal Human Serum/Plasma obtained from healthy donors of US origin. -
表达系统
Native -
Accession
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蛋白长度
Full length protein -
无动物成分
No -
性质
Native -
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种属
Human
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技术指标
Our Abpromise guarantee covers the use of ab205808 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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应用
SDS-PAGE
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形式
Liquid -
补充说明
Origin: Raw material has been tested for HIV-AG and found to be non-reactive. Donor serum has been tested and found to be negative for HIV ½, Hepatitis B Core Antigen, Hepatitis B Surface Antigen, and Hepatitis C Virus by currently approved FDA methods
For in vitro Laboratory Use Only. Not for diagnostic or therapeutic use. Not for human or animal consumption. Suggested applications of our products are not recommendations to use our products in violation of any target restriction or as a license under any target restriction of Abcam.
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Concentration information loading...
制备和贮存
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稳定性和存储
Shipped at 4°C. Store at 4°C (stable for up to 12 months). Upon delivery aliquot. Store at +4°C.
pH: 7.20
Preservative: 0.05% Sodium azide
Constituents: 0.16% Sodium phosphate, 0.87% Sodium chloride
常规信息
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别名
- alb
- ALBU_HUMAN
- Albumin
see all -
功能
Serum albumin, the main protein of plasma, has a good binding capacity for water, Ca(2+), Na(+), K(+), fatty acids, hormones, bilirubin and drugs. Its main function is the regulation of the colloidal osmotic pressure of blood. Major zinc transporter in plasma, typically binds about 80% of all plasma zinc. -
组织特异性
Plasma. -
疾病相关
Defects in ALB are a cause of familial dysalbuminemic hyperthyroxinemia (FDH) [MIM:103600]. FDH is a form of euthyroid hyperthyroxinemia that is due to increased affinity of ALB for T(4). It is the most common cause of inherited euthyroid hyperthyroxinemia in Caucasian population. -
序列相似性
Belongs to the ALB/AFP/VDB family.
Contains 3 albumin domains. -
翻译后修饰
Kenitra variant is partially O-glycosylated at Thr-620. It has two new disulfide bonds Cys-600 to Cys-602 and Cys-601 to Cys-606.
Glycated in diabetic patients.
Phosphorylation sites are present in the extracelllular medium.
Acetylated on Lys-223 by acetylsalicylic acid. -
细胞定位
Secreted. - Information by UniProt
实验方案
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
数据表及文件
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SDS download
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Datasheet download
文献 (4)
ab205808 被引用在 4 文献中.
- Shola David M & Kanayeva D Enzyme linked oligonucleotide assay for the sensitive detection of SARS-CoV-2 variants. Front Cell Infect Microbiol 12:1017542 (2022). PubMed: 36250054
- Kurmangali A et al. Sensitive Detection of SARS-CoV-2 Variants Using an Electrochemical Impedance Spectroscopy Based Aptasensor. Int J Mol Sci 23:N/A (2022). PubMed: 36361926
- Zhao B et al. Single-step, wash-free digital immunoassay for rapid quantitative analysis of serological antibody against SARS-CoV-2 by photonic resonator absorption microscopy. Talanta 225:122004 (2021). PubMed: 33592744
- Vatine GD et al. Human iPSC-Derived Blood-Brain Barrier Chips Enable Disease Modeling and Personalized Medicine Applications. Cell Stem Cell 24:995-1005.e6 (2019). PubMed: 31173718