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Septin 9 抗体

SEPT9 适用: 人, 小鼠, 大鼠 IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7264674
发货至: 中国
  • 抗原 See all Septin 9 (SEPT9) 抗体
    Septin 9 (SEPT9)
    适用
    • 27
    • 6
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 23
    • 4
    克隆类型
    • 26
    • 1
    多克隆
    标记
    • 20
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Septin 9 antibody is un-conjugated
    应用范围
    • 16
    • 9
    • 6
    • 5
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    Immunofluorescence (IF)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human 44083 (NP_001106964.1).
    亚型
    IgG
    Top Product
    Discover our top product SEPT9 Primary Antibody
  • 应用备注
    IF 1:50-1:200
    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
    Septin 9 (SEPT9)
    别名
    SEPT9 (SEPT9 产品)
    别名
    SEPT9 antibody, msf antibody, msf1 antibody, napb antibody, sint1 antibody, pnutl4 antibody, septd1 antibody, af17q25 antibody, septin-9 antibody, AF17q25 antibody, MSF antibody, MSF1 antibody, NAPB antibody, PNUTL4 antibody, SINT1 antibody, SeptD1 antibody, Msf antibody, Sint1 antibody, Eseptin antibody, Slpa antibody, cb999 antibody, fb02h06 antibody, sept9 antibody, wu:fb02h06 antibody, septin 9 antibody, septin-9 antibody, septin 9 S homeolog antibody, septin 9a antibody, SEPT9 antibody, sept9 antibody, LOC100605286 antibody, sept9.S antibody, Sept9 antibody, sept9a antibody
    背景
    This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.
    基因ID
    10801
    UniProt
    Q9UHD8
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