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Separase Antikörper (AA 1866-1966)

Der Maus Monoklonal Anti-Separase-Antikörper wurde für WB validiert. Er ist geeignet, Separase in Proben von Human zu detektieren.
Produktnummer ABIN5540331

Kurzübersicht für Separase Antikörper (AA 1866-1966) (ABIN5540331)

Target

Alle Separase (ESPL1) Antikörper anzeigen
Separase (ESPL1) (Extra Spindle Poles Like 1 (ESPL1))

Reaktivität

  • 91
  • 9
  • 1
Human

Wirt

  • 88
  • 3
  • 1
Maus

Klonalität

  • 89
  • 3
Monoklonal

Konjugat

  • 28
  • 9
  • 9
  • 8
  • 5
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Separase Antikörper ist unkonjugiert

Applikation

  • 47
  • 38
  • 26
  • 26
  • 18
  • 13
  • 12
  • 7
  • 6
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)

Klon

XJ11-1B12
  • Bindungsspezifität

    • 17
    • 15
    • 15
    • 9
    • 6
    • 6
    • 6
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1866-1966

    Spezifität

    This antibody reacts with human Separase (190 kDa).

    Kreuzreaktivität (Details)

    Does not work with Mouse (WR19L, U937, P19, NIH/3T3) and Hamster (CHO).

    Aufreinigung

    Protein A agarose

    Immunogen

    Separase (1866-1966 aa)

    Isotyp

    IgG1
  • Applikationshinweise

    Western blot: 1 μg/mL for chemiluminescence detection system. Not reconmmended for Immunoprecipitation, Immunohistochemistry, and Immunocytochemistry.

    Protokoll

    SDS-PAGE & Western Blotting 1) Wash the cells 3 times with PBS and suspend with 10 volume of cold Lysis buffer (50 mM Tris-HCl, pH 7.2, 250 mM NaCl, 0.1 % NP-40, 2 mM EDTA, 10 % glycerol) containing appropriate protease inhibitors. Incubate it at 4 o C with rotating for 30 minutes, then sonicate briefly (up to 10 seconds). 2) Centrifuge the tube at 12,000 x g for 10 minutes at 4 o C and transfer the supernatant to another tube. Measure the protein concentration of the supernatant and add the Lysis buffer to make 8 mg/mL solution. 3) Mix the sample with equal volume of Laemmli's sample buffer. 4) Boil the samples for 2 minutes and centrifuge. Load 10 μ L of the sample per lane in a 1 mm thick SDS-polyacrylamide gel for electrophoresis. 5) Blot the protein to a polyvinylidene difluoride (PVDF) membrane at 1 mA/cm 2 for 1 hour in a semi-dry transfer system (Transfer Buffer: 25 mM Tris, 190 mM glycine, 20 % MeOH). See the manufacture's manual for precise transfer procedure. 6) To reduce nonspecific binding, soak the membrane in 10 % skimmed milk (in PBS, pH 7.2) for 1 hour at room temperature, or overnight at 4 o C. 7) Incubate the membrane with primary antibody diluted with PBS, pH 7.2 containing 1 % skimmed milk as suggest in the APPLICATIONS for 1 hour at ro om temperature. (The concentration of antibody will depend on condition.) 8) Wash the membrane with PBS-T [0.05 % Tween-20 in PBS] (5 minutes x 3 times). 9) Incubate the membrane with the 1:10,000 HRP-conjugated anti-mouse IgG diluted with 1 % skimmed milk (in PBS, pH 7.2) for 1 hour at room temperature. 10) Wash the membrane with PBS-T (5 minutes x 6 times). 11) Wipe excess buffer on the membrane, then incubate it with appropriate chemilumin escence reagent for 1 minute. Remove extra reagent from the membrane by dabbing with paper towel, and seal it in plastic wrap. 12) Expose to an X-ray film in a dark room for 10 minutes. Develop the film as usual. The condition for exposure and development may vary. (Positive controls for Western blotting HeLa, Raji, ZR-75-1, MCF-7, HL-60, Jurkat)

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS containing 50 % glycerol, pH 7.2. No preservative is contained.

    Konservierungsmittel

    Azide free

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Upon receipt, store undiluted (in aliquots) at -20°C. Avoid repeated freezing and thawing. Shelf life: One year from despatch.
  • Target

    Separase (ESPL1) (Extra Spindle Poles Like 1 (ESPL1))

    Andere Bezeichnung

    separin,espl1

    Hintergrund

    Separase (190 kDa) is a cysteine protease that is essential for chromosome segregation. During cell division the sister chromatids are held together by the cohesin complex. At the onset of anaphase, separase cleaves the SCC1/RAD21 subunit of cohesin, allowing the chromatids to separate and divide with the cell. During most of the cell cycle, separase is inactivated by the securin/PDS-1 protein, which probably covers its active site. Separase is also down re gulated by self-cleavage to a ~65 kDa form. Separase can be used as a marker for centrosomes in mitotic cells.

    UniProt

    Q14674
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