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SRGAP3 抗体

SRGAP3 适用: 人, 小鼠 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7237712
发货至: 中国
  • 抗原 See all SRGAP3 抗体
    SRGAP3 (SLIT-ROBO rho GTPase Activating Protein 3 (SRGAP3))
    适用
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    人, 小鼠
    宿主
    • 17
    克隆类型
    • 17
    多克隆
    标记
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    This SRGAP3 antibody is un-conjugated
    应用范围
    • 7
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    ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human SRGAP3
    亚型
    IgG
    Top Product
    Discover our top product SRGAP3 Primary Antibody
  • 应用备注
    IHC 1:25-1:100
    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
    SRGAP3 (SLIT-ROBO rho GTPase Activating Protein 3 (SRGAP3))
    别名
    SRGAP3 (SRGAP3 产品)
    别名
    AI452337 antibody, Arhgap14 antibody, D130026O08Rik antibody, Gbi antibody, MEGAP antibody, WRP antibody, mKIAA0411 antibody, RGD1563152 antibody, ARHGAP14 antibody, SRGAP2 antibody, RGD1566016 antibody, srGAP2 antibody, fnbp2 antibody, srgap2 antibody, SLIT-ROBO Rho GTPase activating protein 3 antibody, SLIT-ROBO Rho GTPase activating protein 2 antibody, SLIT-ROBO Rho GTPase activating protein 2 L homeolog antibody, Srgap3 antibody, SRGAP3 antibody, Srgap2 antibody, srgap3 antibody, srgap2.L antibody
    背景
    SRGAP3 is a 1099 amino acid protein containing 1 FCH domain, 1 Rho-GAP domain and 1 SH3 domain. Expressed highly in brain, and in lower levels in kidney, WRP is thought to play a role in cell migration through its interaction with Cdc42 and Rac1. Cdc42 and Rac1 are two intracellular signaling proteins that regulate the multistep cell migration process. WRP downregulates Cdc42 and Rac1 activity, thereby impairing actin and microtubule dynamics, the formation of protrusions, and total cell migration. Defects in the gene encoding WRP have been linked to severe idiopathic mental retardation. Three isoforms of WRP exist as a result of alternative splicing events.
    UniProt
    O43295
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