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Septin 9 antibody (AA 1-110)

The Rabbit Polyclonal anti-Septin 9 antibody has been validated for WB and IF. It is suitable to detect Septin 9 in samples from Human.
Catalog No. ABIN6147560

Quick Overview for Septin 9 antibody (AA 1-110) (ABIN6147560)

Target

See all Septin 9 (SEPT9) Antibodies
Septin 9 (SEPT9)

Reactivity

  • 30
  • 8
  • 6
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 26
  • 4
Rabbit

Clonality

  • 29
  • 1
Polyclonal

Conjugate

  • 23
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Septin 9 antibody is un-conjugated

Application

  • 17
  • 11
  • 7
  • 6
  • 5
  • 5
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-110

    Sequence

    MEPPASKVPE VPTAPATDAA PKRVEIQMPK PAEAPTAPSP AQTLENSEPA PVSQLQSRLE PKPQPPVAEA TPRSQEATEA APSCVGDMAD TPRDAGLKQA PASRNEKAPV

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-110 of human Septin 9 (NP_001106964.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IF,1:50 - 1:200

    Comment

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Septin 9 (SEPT9)

    Alternative Name

    9-Sep

    Background

    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.,SEPT9,AF17q25,MSF,MSF1,NAPB,PNUTL4,SINT1,SeptD1,septin-9,Cell Biology & Developmental Biology,Cell Cycle,Immunology & Inflammation,Cytokines,9-Sep

    Molecular Weight

    38 kDa/41 kDa/47 kDa/52 kDa/63 kDa/64 kDa/65 kDa

    Gene ID

    10801

    UniProt

    Q9UHD8
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