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MAP2 Antikörper (AA 19-219)

Dieses Anti-MAP2-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von MAP2 in WB, IHC, IP und IF. Geeignet für Human, Maus und Ratte. Dieses Primary Antibody wurde in 2+ Publikationen zitiert.
Produktnummer ABIN967986

Kurzübersicht für MAP2 Antikörper (AA 19-219) (ABIN967986)

Target

Alle MAP2 Antikörper anzeigen
MAP2 (Microtubule-Associated Protein 2 (MAP2))

Reaktivität

  • 149
  • 96
  • 93
  • 28
  • 25
  • 5
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 119
  • 52
  • 9
  • 2
Maus

Klonalität

  • 130
  • 51
Monoklonal

Konjugat

  • 101
  • 15
  • 13
  • 5
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser MAP2 Antikörper ist unkonjugiert

Applikation

  • 136
  • 74
  • 43
  • 41
  • 39
  • 39
  • 32
  • 30
  • 30
  • 22
  • 21
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunoprecipitation (IP), Immunofluorescence (IF)

Klon

18-MAP2B
  • Bindungsspezifität

    • 17
    • 16
    • 15
    • 15
    • 11
    • 8
    • 7
    • 7
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 19-219

    Kreuzreaktivität

    Ratte (Rattus), Maus

    Produktmerkmale

    1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
    2. Please refer to us for technical protocols.
    3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
    4. Source of all serum proteins is from USDA inspected abattoirs located in the United States.

    Aufreinigung

    The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.

    Immunogen

    Human MAP2B aa. 19-219

    Isotyp

    IgG1 kappa
  • Applikationshinweise

    Methanol Procedure for a 96 well plate: Remove media from wells. Add 100 µl/well fresh 3.7% Formaldehyde in PBS. Incubate for 10 minutes at room temperature (RT). Flick out and add 100 µl/well 90% methanol. Incubate for 5 minutes at RT. Flick out and wash twice with PBS. Flick out PBS and add 100 µl/well blocking buffer (3% FBS in PBS). Incubate for 30 minutes at RT. Flick out and add diluted antibody (diluted in blocking buffer). Incubate for 1 hour at RT. Wash three times with PBS. Flick out PBS and add second step reagent. Incubate for 1 hour at RT. Wash three times with PBS.
    Triton-X 100 Procedure for a 96 well plate: Remove media from wells. Add 100 µl/well fresh 3.7% Formaldehyde in PBS. Incubate for 10 minutes at room temperature (RT). Flick out and add 100 µl/well 0.1% Triton-X 100. Incubate for 5 minutes at RT. Flick out and wash twice with PBS. Flick out PBS and add 100 µl/well blocking buffer (3% FBS in PBS). Incubate for 30 minutes at RT. Flick out and add diluted antibody (diluted in blocking buffer). Incubate for 1 hour at RT. Flick out and wash three times with PBS. Flick out and add second step reagent. Incubate for 1 hour at RT. Flick out and wash three times with PBS.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    250 μg/mL

    Buffer

    Aqueous buffered solution containing BSA, glycerol, and ≤0.09 % sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store undiluted at -20° C.
  • Kanaani, el-Husseini, Aguilera-Moreno, Diacovo, Bredt, Baekkeskov: "A combination of three distinct trafficking signals mediates axonal targeting and presynaptic clustering of GAD65." in: The Journal of cell biology, Vol. 158, Issue 7, pp. 1229-38, (2002) (PubMed).

    Kindler, Schulz, Goedert, Garner: "Molecular structure of microtubule-associated protein 2b and 2c from rat brain." in: The Journal of biological chemistry, Vol. 265, Issue 32, pp. 19679-84, (1991) (PubMed).

  • Target

    MAP2 (Microtubule-Associated Protein 2 (MAP2))

    Andere Bezeichnung

    MAP2B

    Hintergrund

    Microtubule-associated proteins (MAPs) play a crucial role in the development and structure of nerve cells. These proteins are important for the assembly and stability of microtubules during neurite outgrowth and for the morphology of neuronal processes, such as dendrites, MAP2, specifically localized in dendrites, has four known isoforms produced by alternative splicing of the transcript. These isoforms, MAPs A, B, C, and D, are expressed at various stages of neuronal development. MAP2B is a 280-kDa protein expressed throughout brain development. It is composed of several highly conserved domains that are flanked by domains with extensive sequence divergence. An N-terminal conserved domain overlaps with a binding domain for the regulatory subunit of the cAMP-dependent kinase II, while a C-terminal conserved domain overlaps with a microtubule-binding domain. Secondary structure prediction suggests that the portion of MAP2B extending from the microtubule surface is composed of a number of alpha-helices separated by small turns which may account for the extended, yet flexible, structure of MAP2B.

    Molekulargewicht

    280 kDa
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