Fibrillin 1 抗体
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北京 101111
Quick Overview for Fibrillin 1 抗体 (ABIN7238018)
抗原
See all Fibrillin 1 (FBN1) 抗体适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Affinity purification
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免疫原
- Synthetic peptide of human FBN1
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亚型
- IgG
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anti-Fibrillin 1 (FBN1) (AA 246-389) antibody
FBN1 适用: 人 WB, ELISA, ICC, IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Fibrillin 1 (FBN1) (AA 751-895) antibodyFBN1 适用: 大鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Fibrillin 1 (FBN1) (Internal Region) antibodyVerified FBN1 适用: 人 ELISA, IF 宿主: 山羊 Polyclonal unconjugated
anti-Fibrillin 1 (FBN1) (AA 723-902) antibodyFBN1 适用: 人 WB, ELISA, ICC, IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Fibrillin 1 (FBN1) (AA 1703-1889) antibodyFBN1 适用: 小鼠 WB, ELISA, ICC, IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Fibrillin 1 (FBN1) (AA 959-1145) antibodyFBN1 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Fibrillin 1 (FBN1) (AA 168-364) antibodyFBN1 适用: 大鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Fibrillin 1 (FBN1) (AA 401-500) antibodyFBN1 适用: 人, 大鼠 ELISA, IHC (p), IHC (fro), IF (cc), IF (p) 宿主: 兔 Polyclonal unconjugated
anti-Fibrillin 1 (FBN1) (AA 2772-2871) antibodyFBN1 适用: 人 WB, ELISA, IHC (p) 宿主: 小鼠 Monoclonal 3H6 unconjugated
anti-Fibrillin 1 (FBN1) (AA 723-902) antibodyFBN1 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
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应用备注
- IHC 1:50-1:200
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.3 mg/mL
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缓冲液
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- Fibrillin 1 (FBN1)
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别名
- FBN1
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背景
- This gene encodes a member of the fibrillin family. The encoded protein is a large, extracellular matrix glycoprotein that serve as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body. Mutations in this gene are associated witHuman, Mousearfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome.
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NCBI登录号
- NP_000129
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UniProt
- P35555
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途径
- Maintenance of Protein Location, SARS-CoV-2 Protein Interactome
抗原
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