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Filamin A 抗体

FLNA 适用: 人, 小鼠 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7237020
发货至: 中国
  • 抗原 See all Filamin A (FLNA) 抗体
    Filamin A (FLNA) (Filamin A, alpha (FLNA))
    适用
    • 98
    • 25
    • 21
    • 3
    • 1
    • 1
    人, 小鼠
    宿主
    • 90
    • 7
    • 1
    克隆类型
    • 80
    • 18
    多克隆
    标记
    • 46
    • 6
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    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    This Filamin A antibody is un-conjugated
    应用范围
    • 53
    • 32
    • 28
    • 28
    • 27
    • 26
    • 13
    • 11
    • 7
    • 6
    • 4
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human FLNA
    亚型
    IgG
    Top Product
    Discover our top product FLNA Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.6 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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.
  • 抗原
    Filamin A (FLNA) (Filamin A, alpha (FLNA))
    别名
    FLNA (FLNA 产品)
    背景
    The protein encoded by this gene is an actin-binding protein that crosslinks actin filaments and links actin filaments to membrane glycoproteins. The encoded protein is involved in remodeling the cytoskeleton to effect changes in cell shape and migration. This protein interacts with integrins, transmembrane receptor complexes, and second messengers. Defects in this gene are a cause of several syndromes, including periventricular nodular heterotopias (PVNH1, PVNH4), otopalatodigital syndromes (OPD1, OPD2), frontometaphyseal dysplasia (FMD), Melnick-Needles syndrome (MNS), and X-linked congenital idiopathic intestinal pseudoobstruction (CIIPX). Two transcript variants encoding different isoforms have been found for this gene.
    分子量
    281 kDa
    NCBI登录号
    NP_001104026
    UniProt
    P21333
    途径
    TCR Signaling, Maintenance of Protein Location
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