Fibulin 5 抗体
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北京 101111
Quick Overview for Fibulin 5 抗体 (ABIN6572097)
抗原
See all Fibulin 5 (FBLN5) 抗体适用
宿主
克隆类型
标记
应用范围
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纯化方法
- Affinity purification
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免疫原
- Recombinant fusion protein of human FBLN5 (NP_006320.2).
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亚型
- IgG
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anti-Fibulin 5 (FBLN5) (AA 101-200) antibody
FBLN5 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Fibulin 5 (FBLN5) (AA 99-205) antibodyFBLN5 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Fibulin 5 (FBLN5) (AA 199-448) antibodyFBLN5 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Fibulin 5 (FBLN5) antibodyFBLN5 适用: 人 IHC, ELISA 宿主: 小鼠 Monoclonal 3F10A5 unconjugated
anti-Fibulin 5 (FBLN5) (AA 242-448) antibodyFBLN5 适用: 人 IHC, ELISA 宿主: 小鼠 Monoclonal 1G6A4 unconjugated
anti-Fibulin 5 (FBLN5) antibodyFBLN5 适用: 人 WB, FACS 宿主: 兔 Monoclonal 25GB1575 unconjugated Recombinant Antibody
anti-Fibulin 5 (FBLN5) (C-Term) antibodyFBLN5 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Fibulin 5 (FBLN5) antibodyFBLN5 适用: 人, 小鼠 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Fibulin 5 (FBLN5) antibodyFBLN5 适用: 人 ELISA 宿主: 小鼠 Monoclonal 3F8D5 unconjugated
anti-Fibulin 5 (FBLN5) (AA 242-448) antibodyFBLN5 适用: 人 WB, IHC, ELISA 宿主: 小鼠 Monoclonal 1G6A4 unconjugated
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应用备注
- WB 1:500-1:2000 IF 1:50-1:100
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
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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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- Fibulin 5 (FBLN5)
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别名
- FBLN5
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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).
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分子量
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Observed_MW: 70kDa
Calculated_MW: 50kDa
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基因ID
- 10516
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UniProt
- Q9UBX5
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途径
- SARS-CoV-2 Protein Interactome
抗原
-
