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Septin 9 抗体 (Middle Region)

This 兔 多克隆 antibody specifically detects Septin 9 in WB 和 IHC. It exhibits reactivity toward 人, 小鼠, 大鼠, 豚鼠, 斑马鱼, Cow, 犬, 马 和 兔.
产品编号 ABIN2773992
发货至: 中国
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Quick Overview for Septin 9 抗体 (Middle Region) (ABIN2773992)

抗原

See all Septin 9 (SEPT9) 抗体
Septin 9 (SEPT9)

适用

  • 31
  • 7
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  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
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  • 1
人, 小鼠, 大鼠, 豚鼠, 斑马鱼, Cow, 犬, 马, 兔

宿主

  • 27
  • 4

克隆类型

  • 30
  • 1
多克隆

标记

  • 24
  • 1
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This Septin 9 antibody is un-conjugated

应用范围

  • 18
  • 10
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Western Blotting (WB), Immunohistochemistry (IHC)
  • 抗原表位

    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
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    Middle Region

    序列

    VNEKFREMIP FAVVGSDHEY QVNGKRILGR KTKWGTIEVE NTTHCEFAYL

    预测反应

    Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 86%, Rat: 100%, Zebrafish: 92%

    产品特性

    This is a rabbit polyclonal antibody against SEPT9. It was validated on Western Blot using a cell lysate as a positive control.

    纯化方法

    Affinity Purified

    免疫原

    The immunogen is a synthetic peptide directed towards the middle region of human SEPT9
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator.

    说明

    Antigen size: 422 AA

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    Lot specific

    缓冲液

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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.

    注意事项

    Avoid repeated freeze-thaw cycles.

    储存条件

    -20 °C

    储存方法

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 抗原

    Septin 9 (SEPT9)

    别名

    SEPT9

    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.
    Alias Symbols: AF17q25, KIAA0991, MSF, MSF1, NAPB, PNUTL4, SINT1, SeptD1
    Protein Interaction Partner: SEPT6, HAUS1, SUMO2, UBC, EED, HNRNPD, FN1, CFTR, VAMP2, SVIL, SCP2, NDUFV2, NCL, MSH2, HSPD1, FLNB, COPA, SEPT7, APP, UQCRFS1P1, UQCRFS1, TPM3, SUCLG2, VMA21, SEPT11, TMED9, HN1, TOR1AIP1, FERMT2, TIMM44, HRSP12, SCO2, SEC22B, VAPB, SUCLG1, UBXN6, UBD, S
    Protein Size: 422

    分子量

    46 kDa

    基因ID

    10801

    NCBI登录号

    NM_001113492, NP_001106964

    UniProt

    Q9UHD8
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