製品の概要

  • 製品名
  • 製品の詳細
    Rabbit polyclonal to MSF
  • アプリケーション
    適用あり: IHC-Pmore details
  • 種交差性
    交差種: Human
    交差が予測される動物種: Rhesus monkey
  • 免疫原

    Synthetic peptide, corresponding to a region within amino acids 536-586 of Human MSF (NP_001106963.1).

  • ポジティブ・コントロール
    • Human Breast Carcinoma, Colon Carcinoma, Prostate Carcinoma and Stomach Adenocarcinoma tissues.

製品の特性

  • 製品の状態
    Liquid
  • 保存方法
    Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
  • バッファー
    Preservative: 0.09% Sodium azide
    Constituents: 99% Tris buffered saline, 0.1% BSA
  • Concentration information loading...
  • 精製度
    Immunogen affinity purified
  • ポリ/モノ
    ポリクローナル
  • アイソタイプ
    IgG
  • 研究分野

アプリケーション

Our Abpromise guarantee covers the use of ab117832 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

アプリケーション Abreviews 特記事項
IHC-P 1/100 - 1/500. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.

ターゲット情報

  • 機能
    Filament-forming cytoskeletal GTPase (By similarity). May play a role in cytokinesis (Potential). May play a role in the internalization of 2 intracellular microbial pathogens, Listeria monocytogenes and Shigella flexneri.
  • 組織特異性
    Widely expressed. Isoforms are differentially expressed in testes, kidney, liver heart, spleen, brain, peripheral blood leukocytes, skeletal muscle and kidney. Specific isoforms appear to demonstrate tissue specificity. Isoform 5 is the most highly expressed in fetal tissue. Isoform 1 is detected in all tissues except the brain and thymus, while isoform 2, isoform 3, and isoform 4 are detected at low levels in approximately half of the fetal tissues.
  • 関連疾患
    Note=A chromosomal aberration involving SEPT9/MSF is found in therapy-related acute myeloid leukemia (t-AML). Translocation t(11;17)(q23;q25) with MLL.
    Defects in SEPT9 are a cause of hereditary neuralgic amyotrophy (HNA) [MIM:162100]; also known as neuritis with brachial predilection (NAPB) or hereditary brachial plexus neuropathy or hereditary neuralgic amyotrophy with predilection for brachial plexus. HNA is an autosomal dominant form of recurrent focal neuropathy characterized clinically by acute, recurrent episodes of brachial plexus neuropathy with muscle weakness and atrophy preceded by severe pain in the affected arm. HNA is triggered by environmental factors such as infection or parturition.
  • 配列類似性
    Belongs to the septin family.
  • 細胞内局在
    Cytoplasm > cytoskeleton. In an epithelial cell line, concentrates at cell-cell contact areas. After TGF-beta1 treatment and induction of epithelial to mesenchymal transition, colocalizes partly with actin stress fibers. During bacterial infection, displays a collar shape structure next to actin at the pole of invading bacteria.
  • Information by UniProt
  • 参照データベース
  • 別名
    • AF17q25 antibody
    • Cell division control protein septin D1 antibody
    • KIAA0991 antibody
    • MLL septin like fusion protein antibody
    • MLL septin-like fusion protein antibody
    • MLL septin-like fusion protein MSF-A antibody
    • MSF antibody
    • MSF1 antibody
    • NAPB antibody
    • Ov/Br septin antibody
    • Ovarian/breast septin alpha antibody
    • Ovarian/Breast septin antibody
    • PNUTL4 antibody
    • SEPT9 antibody
    • SEPT9_HUMAN antibody
    • SeptD1 antibody
    • Septin 9 antibody
    • Septin D1 antibody
    • Septin-9 antibody
    • SINT1 antibody
    see all

画像

  • Immunofluorescent analysis of Human MSF detection in Paraffin-embedded, Formalin-fixed Human Prostate carcinoma tissue using 1/100 ab117832. Detection:Red-fluorescent Goat anti-Rabbit IgG-heavy and light chain cross-adsorbed Antibody DyLight 594 Conjugated used at a dilution of 1/100.
  • Immunohistochemical analysis of MSF expression in Formalin-fixed, Paraffin-embedded Human breast carcinoma using 1/250 ab117832. Detection: DAB staining.

プロトコール

参考文献

ab117832 has not yet been referenced specifically in any publications.

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