FLNB 抗体
Quick Overview for FLNB 抗体 (ABIN6569221)
抗原
See all FLNB 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 FLNB (NP_001157789.1).
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亚型
- IgG
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anti-Filamin B, beta (FLNB) antibody
FLNB 适用: 人, 小鼠, 大鼠 IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Filamin B, beta (FLNB) (AA 1686-1785) antibodyFLNB 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Filamin B, beta (FLNB) (N-Term) antibodyKO Validated FLNB 适用: 人 WB, IF, ICC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Filamin B, beta (FLNB) (AA 30-239) antibodyFLNB 适用: 人 WB, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Filamin B, beta (FLNB) (AA 1-237) antibodyFLNB 适用: 人 WB, IHC, ICC, IP 宿主: 兔 Polyclonal unconjugated
anti-Filamin B, beta (FLNB) (AA 1551-1650) antibodyFLNB 适用: 人 WB, ELISA, ICC, IF (cc), IF (p), IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Filamin B, beta (FLNB) (AA 2061-2193) antibodyFLNB 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Filamin B, beta (FLNB) (AA 2061-2193) antibodyFLNB 适用: 人 WB, IHC, IP, IF/ICC 宿主: 兔 Polyclonal unconjugated
anti-Filamin B, beta (FLNB) (AA 163-196) antibodyFLNB 适用: 人 WB 宿主: 兔 Polyclonal RB54051 unconjugated
anti-Filamin B, beta (FLNB) (AA 288-322) antibodyFLNB 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal RB54052 unconjugated
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应用备注
- IHC 1:50-1:100 IF 1:20-1:100
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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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- FLNB (Filamin B, beta (FLNB))
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别名
- FLNB
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背景
- This gene encodes a member of the filamin family. The encoded protein interacts with glycoprotein Ib alpha as part of the process to repair vascular injuries. The platelet glycoprotein Ib complex includes glycoprotein Ib alpha, and it binds the actin cytoskeleton. Mutations in this gene have been found in several conditions: atelosteogenesis type 1 and type 3, boomerang dysplasia, autosomal dominant Larsen syndrome, and spondylocarpotarsal synostosis syndrome. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.
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分子量
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Observed_MW: 298kDa
Calculated_MW: 230-281kDa
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基因ID
- 2317
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UniProt
- O75369
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途径
- Maintenance of Protein Location
抗原
-
