电话:
400-7060-959
传真:
+86 10 56315212-8813
电子邮件:
orders@antibodies-online.cn

FLNB 抗体

FLNB 适用: 人, 小鼠, 大鼠 IHC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6569221
发货至: 中国
  • 抗原 See all FLNB 抗体
    FLNB (Filamin B, beta (FLNB))
    适用
    • 45
    • 7
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 40
    • 4
    • 1
    克隆类型
    • 42
    • 3
    多克隆
    标记
    • 27
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FLNB antibody is un-conjugated
    应用范围
    • 42
    • 13
    • 13
    • 12
    • 10
    • 9
    • 8
    • 8
    • 3
    • 2
    • 2
    • 1
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human FLNB (NP_001157789.1).
    亚型
    IgG
    Top Product
    Discover our top product FLNB Primary Antibody
  • 应用备注
    IHC 1:50-1:100 IF 1:20-1:100
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    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.
  • 抗原
    FLNB (Filamin B, beta (FLNB))
    别名
    FLNB (FLNB 产品)
    别名
    ABP-278 antibody, ABP-280 antibody, AOI antibody, FH1 antibody, FLN-B antibody, FLN1L antibody, LRS1 antibody, SCT antibody, TABP antibody, TAP antibody, AL024016 antibody, filamin B antibody, filamin, beta antibody, FLNB antibody, Flnb antibody
    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.
    分子量

    Observed_MW: 298kDa

    Calculated_MW: 230-281kDa

    基因ID
    2317
    UniProt
    O75369
    途径
    Maintenance of Protein Location
You are here:
客服