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TCTN2 抗体 (PE)

TCTN2 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal PE
产品编号 ABIN1712697
发货至: 中国
  • 抗原 See all TCTN2 抗体
    TCTN2 (Tectonic Family Member 2 (TCTN2))
    适用
    • 25
    • 14
    • 7
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 28
    • 1
    克隆类型
    • 28
    • 1
    多克隆
    标记
    • 11
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TCTN2 antibody is conjugated to PE
    应用范围
    • 27
    • 13
    • 13
    • 8
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    交叉反应
    小鼠
    预测反应
    Human,Rat
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human TCTN2
    亚型
    IgG
    Top Product
    Discover our top product TCTN2 Primary Antibody
  • 应用备注
    FCM(1:20-100)
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    有效期
    12 months
  • 抗原
    TCTN2 (Tectonic Family Member 2 (TCTN2))
    别名
    Tctn2 (TCTN2 产品)
    别名
    fb44f11 antibody, wu:fb44f11 antibody, tect2 antibody, C12orf38 antibody, MKS8 antibody, TECT2 antibody, 4432405B04Rik antibody, Tect2 antibody, tectonic family member 2 antibody, TCTN2 antibody, tctn2 antibody, Tctn2 antibody
    背景

    Synonyms: C12orf38, FLJ12975, MKS8, OTTHUMP00000239215, OTTHUMP00000239216, Tctn2, TECT2, TECT2_HUMAN, Tectonic family member 2, Tectonic-2.

    Background: Defects in TCTN2 are the cause of Meckel syndrome type 8 (MKS8) [MIM:613885]. A disorder characterized by a combination of renal cysts and variably associated features including developmental anomalies of the central nervous system (typically encephalocele), hepatic ductal dysplasia and cysts, and polydactyly.

    途径
    Proton Transport
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