Fibulin 5 抗体 (AA 199-448)
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- 抗原 See all Fibulin 5 (FBLN5) 抗体
- Fibulin 5 (FBLN5)
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抗原表位
- AA 199-448
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This Fibulin 5 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (IF)
- 序列
- NEDGRSCQDV NECATENPCV QTCVNTYGSF ICRCDPGYEL EEDGVHCSDM DECSFSEFLC QHECVNQPGT YFCSCPPGYI LLDDNRSCQD INECEHRNHT CNLQQTCYNL QGGFKCIDPI RCEEPYLRIS DNRCMCPAEN PGCRDQPFTI LYRDMDVVSG RSVPADIFQM QATTRYPGAY YIFQIKSGNE GREFYMRQTG PISATLVMTR PIKGPREIQL DLEMITVNTV INFRGSSVIR LRIYVSQYPF
- 交叉反应
- 人, 小鼠, 大鼠
- 产品特性
- Polyclonal Antibodies
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 199-448 of human FBLN5 (NP_006320.2).
- 亚型
- IgG
- Top Product
- Discover our top product FBLN5 Primary Antibody
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- 应用备注
- WB,1:500 - 1:2000,IF,1:50 - 1:100
- 说明
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HIGH QUALITY
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- Fibulin 5 (FBLN5)
- 别名
- FBLN5 (FBLN5 产品)
- 别名
- zgc:103575 antibody, FBLN5 antibody, MGC108414 antibody, Fibulin-5 antibody, DKFZp469K0327 antibody, ADCL2 antibody, ARCL1A antibody, ARMD3 antibody, DANCE antibody, EVEC antibody, FIBL-5 antibody, UP50 antibody, A55 antibody, fibulin 5 antibody, fbln5 antibody, FBLN5 antibody, Fbln5 antibody
- 背景
- The protein encoded by this gene is a secreted, extracellular matrix protein containing an Arg-Gly-Asp (RGD) motif and calcium-binding EGF-like domains. It promotes adhesion of endothelial cells through interaction of integrins and the RGD motif. It is prominently expressed in developing arteries but less so in adult vessels. However, its expression is reinduced in balloon-injured vessels and atherosclerotic lesions, notably in intimal vascular smooth muscle cells and endothelial cells. Therefore, the protein encoded by this gene may play a role in vascular development and remodeling. Defects in this gene are a cause of autosomal dominant cutis laxa, autosomal recessive cutis laxa type I (CL type I), and age-related macular degeneration type 3 (ARMD3).,FBLN5,ADCL2,ARCL1A,ARMD3,DANCE,EVEC,FIBL-5,HNARMD,UP50,fibulin-5,Signal Transduction,Cell Biology & Developmental Biology,Cell Adhesion,Cell Adhesion Molecules,Cytoskeleton,Extracellular Matrix,Cardiovascular,Cardiovascular diseases,Hypertension,FBLN5
- 分子量
- 50 kDa
- 基因ID
- 10516
- UniProt
- Q9UBX5
- 途径
- SARS-CoV-2 Protein Interactome
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