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Septin 9 antibody (AA 203-253)

This Rabbit Polyclonal antibody specifically detects Septin 9 in WB and ELISA. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN8124587
$385.00
Plus shipping costs $50.00
50 μL
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Septin 9 antibody (AA 203-253) (ABIN8124587)

Target

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

Reactivity

  • 45
  • 21
  • 7
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Mouse, Rat

Host

  • 41
  • 4
Rabbit

Clonality

  • 44
  • 1
Polyclonal

Conjugate

  • 28
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Septin 9 antibody is un-conjugated

Application

  • 23
  • 14
  • 14
  • 10
  • 10
  • 7
  • 5
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

    • 13
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 203-253

    Purpose

    SEPT9 Antibody

    Specificity

    SEPT9 Polyclonal Antibody detects endogenous levels of protein.

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Immunogen

    Synthesized peptide derived from part region of human protein AA range: 203-253

    Isotype

    IgG
  • Application Notes

    WB 1:500-2000 ELISA 1:5000-20000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid in PBS containing 50 % glycerol, and 0.02 % sodium azide.

    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/1 year

    Expiry Date

    12 months
  • Target

    Septin 9 (SEPT9)

    Alternative Name

    SEPT9

    Background

    Background: septin 9(SEPT9) Homo sapiens 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.[provided by RefSeq, Mar 2009],

    Gene Name: SEPT9 KIAA0991 MSF

    Protein Name: Septin-9 (MLL septin-like fusion protein MSF-A) (MLL septin-like fusion protein) (Ovarian/Breast septin) (Ov/Br septin) (Septin D1)

    Gene ID

    10801

    UniProt

    Q9UHD8
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