SEPT9 monoclonal antibody (M01), clone 2C6

Catalog # H00010801-M01

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Size:100 ug
Price: USD $ 335.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Sandwich ELISA (Recombinant protein)
Application

Sandwich ELISA (Recombinant protein)

Detection limit for recombinant GST tagged SEPT9 is 0.03 ng/ml as a capture antibody.

QC Test

Western Blot detection against Immunogen (36.41 KDa) .

  • Specification

    Product Description

    Mouse monoclonal antibody raised against a partial recombinant SEPT9.

    Immunogen

    SEPT9 (AAH21192, 26 a.a. ~ 125 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

    Sequence

    PRRVQTPLLRATVASSTQKFQDLGVKNSEPSARHVDSLSQRSPKASLRRVELSGPKAAEPVSRRTELSIDISSKQVENAGAIGPSRFGLKRAEVLGHKTP

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (90); Rat (89)

    Isotype

    IgG2a Kappa

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Western Blot detection against Immunogen (36.41 KDa) .

    Storage Buffer

    In 1x PBS, pH 7.4

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Recombinant protein)

    Sandwich ELISA (Recombinant protein)

    Detection limit for recombinant GST tagged SEPT9 is 0.03 ng/ml as a capture antibody.

    ELISA

  • Gene Info — SEPT9

    Entrez GeneID

    10801

    GeneBank Accession#

    BC021192

    Protein Accession#

    AAH21192

    Gene Name

    SEPT9

    Gene Alias

    AF17q25, FLJ75490, KIAA0991, MSF, MSF1, NAPB, PNUTL4, SINT1, SeptD1

    Gene Description

    septin 9

    Omim ID

    162100 604061

    Gene Ontology

    Hyperlink

    Gene Summary

    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

    Other Designations

    MLL septin-like fusion|Ov/Br septin|ovarian/breast septin|septin D1

  • Interactome
  • Disease
  • Publication Reference
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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