电话:
+86 (0512) 65829739
传真:
+86 (010) 6788 5057
电子邮件:
orders@antibodies-online.cn

FLNB 抗体

FLNB 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7114241
发货至: 中国
  • 抗原 See all FLNB 抗体
    FLNB (Filamin B, beta (FLNB))
    适用
    • 43
    • 7
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 38
    • 4
    • 1
    克隆类型
    • 40
    • 3
    多克隆
    标记
    • 26
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FLNB antibody is un-conjugated
    应用范围
    • 40
    • 13
    • 13
    • 10
    • 9
    • 9
    • 8
    • 7
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    纯化方法
    Immunogen affinity purified
    纯度
    ≥95 % as determined by SDS-PAGE
    免疫原
    filamin B, beta (actin binding protein 278)
    亚型
    IgG
    Top Product
    Discover our top product FLNB Primary Antibody
  • 应用备注
    WB: 1:500 - 1:1000, IHC: 1:20 - 1:50
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    PBS with 0.02 % sodium azide and 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
    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
    有效期
    12 months
  • 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
    Synonyms:FLN1L, FLN3, TABP, TAP Background: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
    298 kDa
    基因ID
    2317
    UniProt
    O75369
    途径
    Maintenance of Protein Location
You are here:
客服