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FLNB 抗体 (N-Term)

This anti-FLNB antibody is a 小鼠 单克隆 antibody detecting FLNB in WB 和 IHC (p). Suitable for 人.
产品编号 ABIN7464198
发货至: 中国

Quick Overview for FLNB 抗体 (N-Term) (ABIN7464198)

抗原

See all FLNB 抗体
FLNB (Filamin B, beta (FLNB))

适用

  • 54
  • 9
  • 5
  • 2
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  • 1
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  • 1
  • 1
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宿主

  • 48
  • 5
  • 1
小鼠

克隆类型

  • 49
  • 5
单克隆

标记

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  • 4
  • 2
  • 1
  • 1
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  • 1
  • 1
  • 1
  • 1
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This FLNB antibody is un-conjugated

应用范围

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  • 20
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  • 3
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  • 1
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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

质量等级

KO Validated

克隆位点

GT1282
  • 抗原表位

    • 15
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
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    • 1
    • 1
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    N-Term

    交叉反应

    人, 大鼠

    纯化方法

    Affinity purified by Protein G.

    免疫原

    Recombinant protein encompassing a sequence within the N-terminus region of human Filamin B. The exact sequence is proprietary.

    亚型

    IgG1
  • 应用备注

    WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: 293T , A431 , HeLa , HepG2

    Validation: KO/KD

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1.83 mg/mL

    缓冲液

    PBS, No Preservative

    储存液

    Without preservative

    储存条件

    4 °C,-20 °C

    储存方法

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    FLNB (Filamin B, beta (FLNB))

    别名

    filamin B

    背景

    Filamin B , ABP-278 , ABP-280 , AOI , FH1 , FLN-B , FLN1L , LRS1 , SCT , TABP , TAP,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. [provided by RefSeq]

    分子量

    278 kDa

    基因ID

    2317

    UniProt

    O75369

    途径

    Maintenance of Protein Location
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