CST3 抗体
Quick Overview for CST3 抗体 (ABIN7148973)
抗原
See all CST3 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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交叉反应
- 人
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纯化方法
- Protein G purified
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免疫原
- Recombinant Human Cystatin C protein
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亚型
- IgG2b
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anti-Cystatin C (CST3) antibody
CST3 适用: 人 WB, ELISA, IHC (p), IF 宿主: 小鼠 Monoclonal 3B6 unconjugated
anti-Cystatin C (CST3) antibodyCST3 适用: 人, 小鼠, 大鼠, 猴 WB, ELISA, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Cystatin C (CST3) antibodyCST3 适用: 人 WB, IF 宿主: 小鼠 Monoclonal 1A6 unconjugated
anti-Cystatin C (CST3) antibodyCST3 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 5H2 unconjugated
anti-Cystatin C (CST3) (C-Term) antibodyVerified CST3 适用: 小鼠 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Cystatin C (CST3) (Internal Region) antibodyVerified CST3 适用: 人 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Cystatin C (CST3) (Internal Region) antibodyCST3 适用: 人, 小鼠, 大鼠, 猴 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Cystatin C (CST3) (AA 1-146) antibodyCST3 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Cystatin C (CST3) (AA 28-127) antibodyCST3 适用: 人 ELISA 宿主: 小鼠 Monoclonal 3D10 unconjugated
anti-Cystatin C (CST3) antibodyCST3 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1H4 unconjugated
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应用备注
- Recommended dilution:IHC:1:50-1:500,
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
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Preservative: 0.03 % Proclin 300
Constituents: 50 % Glycerol, 0.01M PBS, PH 7.4 -
储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C,-80 °C
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储存方法
- Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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- CST3 (Cystatin C (CST3))
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别名
- CST3
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背景
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Background: Defects in CST3 are the cause of amyloidosis type 6 (AMYL6) [MIM:105150], also known as hereditary cerebral hemorrhage with amyloidosis (HCHWA), cerebral amyloid angiopathy (CAA) or cerebroarterial amyloidosis Icelandic type. AMYL6 is a hereditary generalized amyloidosis due to cystatin C amyloid deposition. Cystatin C amyloid accumulates in the walls of arteries, arterioles, and sometimes capillaries and veins of the brain, and in various organs including lymphoid tissue, spleen, salivary glands, and seminal vesicles. Amyloid deposition in the cerebral vessels results in cerebral amyloid angiopathy, cerebral hemorrhage and premature stroke. Cystatin C levels in the cerebrospinal fluid are abnormally low.Genetic variations in CST3 are associated with age-related macular degeneration type 11 (ARMD11) [MIM:611953]. ARMD is a multifactorial eye disease and the most common cause of irreversible vision loss in the developed world. In most patients, the disease is manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid that lie beneath the retinal pigment epithelium and within an elastin-containing structure known as Bruch membrane.
Aliases: CysC,Cystatin-3,Gamma-trace,Neuroendocrine basic polypeptide,Post-gamma-globulin
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UniProt
- P01034
抗原
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