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TUBA1B anticorps

L’anticorps Souris Monoclonal anti-TUBA1B a été validé pour WB, IF, IHC (p), IHC (fro), IP et EIA. Il convient pour détecter TUBA1B dans des échantillons de Toutes les espèces. Il y a 11+ publications disponibles.
N° du produit ABIN112505

Aperçu rapide pour TUBA1B anticorps (ABIN112505)

Antigène

Voir toutes TUBA1B Anticorps
TUBA1B (Tubulin, alpha 1B (TUBA1B))

Reactivité

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Toutes les espèces

Hôte

  • 45
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  • 1
Souris

Clonalité

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  • 19
Monoclonal

Conjugué

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Cet anticorp TUBA1B est non-conjugé

Application

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Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunoprecipitation (IP), Enzyme Immunoassay (EIA)

Clone

TU-01
  • Specificité

    The antibody recognizes the defined epitope (aa 65-97) on N-terminal structural domain of alpha Tubulin. Reacts with all species (recognized epitope conserved within all species).

    Purification

    Precipitation Methods

    Immunogène

    Fraction of tubulin purified from pig brain by two cycles of polymerization-depolymerization

    Isotype

    IgG1
  • Indications d'application

    Western Blotting (Reducing conditions): Recommended Dilution: 1-2 μg/mL,Incubation Time: 60 min, room temperature. Positive Control: HPB-ALL peripheral blood leukemia cell lysate (incubation 60 min)Porcine brain lysate (incubation 90 min). Sample preparation: Resuspend approx.50 mil. cells in 1 mLcold Lysis buffer(1 % laurylmaltoside in 20 mM Tris/Cl, 100 mM NaCl pH 8.2, 50 mM NaF including Proteaseinhibitor Cocktail). Incubate 60 min on ice. Centrifuge to remove cell debris. Mix lysatewith reducing Laemmli SDS-PAGE sample buffer. Immunocytochemistry: Recommended Dilution: DY547 conjugate: 2-3 μg/mL, FITC conjugate: 3 μg/mL. Staining technique: fixed and permeabilized cells. Clone TU-01 has also been described to work in Immunohistochemistry, ELISA andImmunoprecipitation.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    Restrictions

    For Research Use only
  • Concentration

    1.0 mg/mL

    Buffer

    PBS, pH ~7.4, 15 mM Sodium Azide

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Lukas, Mazna, Valenta, Doubravska, Pospichalova, Vojtechova, Fafilek, Ivanek, Plachy, Novak, Korinek: "Dazap2 modulates transcription driven by the Wnt effector TCF-4." dans: Nucleic acids research, Vol. 37, Issue 9, pp. 3007-20, (2009) (PubMed).

    Eisendle, Grabner, Kutzner, Zelger: "Possible role of Borrelia burgdorferi sensu lato infection in lichen sclerosus." dans: Archives of dermatology, Vol. 144, Issue 5, pp. 591-8, (2008) (PubMed).

    Kukharskyy, Sulimenko, Mac?rek, Sulimenko, Dráberová, Dráber: "Complexes of gamma-tubulin with nonreceptor protein tyrosine kinases Src and Fyn in differentiating P19 embryonal carcinoma cells." dans: Experimental cell research, Vol. 298, Issue 1, pp. 218-28, (2004) (PubMed).

    Smertenko, Blume, Viklický, Dráber: "Exposure of tubulin structural domains in Nicotiana tabacum microtubules probed by monoclonal antibodies." dans: European journal of cell biology, Vol. 72, Issue 2, pp. 104-12, (1997) (PubMed).

    Smertenko, Blume, Viklický, Opatrný, Dráber: "Post-translational modifications and multiple tubulin isoforms in Nicotiana tabacum L. cells." dans: Planta, Vol. 201, Issue 3, pp. 349-58, (1997) (PubMed).

    Nováková, Dráberová, Schürmann, Czihak, Viklický, Dr-aber: "gamma-Tubulin redistribution in taxol-treated mitotic cells probed by monoclonal antibodies." dans: Cell motility and the cytoskeleton, Vol. 33, Issue 1, pp. 38-51, (1996) (PubMed).

    Linhartová, Dráber, Dráberová, Viklický: "Immunological discrimination of beta-tubulin isoforms in developing mouse brain. Post-translational modification of non-class-III beta-tubulins." dans: The Biochemical journal, Vol. 288 ( Pt 3), pp. 919-24, (1993) (PubMed).

    Dráber, Dráberová, Viklický: "Immunostaining of human spermatozoa with tubulin domain-specific monoclonal antibodies. Recognition of a unique beta-tubulin epitope in the sperm head." dans: Histochemistry, Vol. 95, Issue 5, pp. 519-24, (1991) (PubMed).

    Dráber, Dráberová, Linhartová, Viklický: "Differences in the exposure of C- and N-terminal tubulin domains in cytoplasmic microtubules detected with domain-specific monoclonal antibodies." dans: Journal of cell science, Vol. 92 ( Pt 3), pp. 519-28, (1990) (PubMed).

    Grimm, Breitling, Little: "Location of the epitope for the alpha-tubulin monoclonal antibody TU-O1." dans: Biochimica et biophysica acta, Vol. 914, Issue 1, pp. 83-8, (1987) (PubMed).

    Dráber, Dráberová, Zicconi, Sellitto, Viklický, Cappuccinelli: "Heterogeneity of microtubules recognized by monoclonal antibodies to alpha-tubulin." dans: European journal of cell biology, Vol. 41, Issue 1, pp. 82-8, (1987) (PubMed).

  • Antigène

    TUBA1B (Tubulin, alpha 1B (TUBA1B))

    Autre désignation

    alpha Tubulin / TUBA1B

    Sujet

    The microtubules are intracellular dynamic polymers made up of evolutionarily conserved polymorphic alpha/beta-tubulin heterodimers and a large number of microtubule-associated proteins (MAPs). The microtubules consist of 13 protofilaments and have an outer diameter 25 nm. Microtubules have their intrinsic polarity, highly dynamic plus ends and less dynamic minus ends. Microtubules are required for vital processes in eukaryotic cells including mitosis, meiosis, maintenance of cell shape and intracellular transport. Microtubules are also necessary for movement of cells by means of flagella and cilia. In mammalian tissue culture cells microtubules have their minus ends anchored in microtubule organizing centers (MTOCs).The GTP (guanosintriphosphate) molecule is an essential for tubulin heterodimer to associate with other heterodimers to form microtubule. In vivo, microtubule dynamics vary considerably. Microtubule polymerization is reversible and a populations of microtubules in cells are on their minus ends either growing or shortening, this phenomenon is called dynamic instability of microtubules. On a practical level, microtubules can easily be stabilized by the addition of non-hydrolysable analogues of GTP (eg. GMPPCP) or morecommonly by anti-cancer drugs such as Taxol. Taxol stabilizes microtubules at room temperature for many hours. Using limited proteolysis by enzymes both tubulin subunits can be divided into N-terminal and C-terminal structural domains. The alpha-tubulin (relative molecular weight about 50 kDa) is globular protein that exists in cells as part of soluble alpha/beta-tubulin dimer or it is polymerized into microtubules. In different species it is coded by multiple tubulin genes that form tubulin classes (in human 6 genes). Expressed tubulin genes are named tubulin isotypes. Some of the tubulin isotypes are expressed ubiquitously, while some have more restricted tissue expression. Alpha-tubulin is also subject of numerous post-translational modifications. Tubulin isotypes and their posttranslational modifications are responsible for multiple tubulin charge variants - tubulin isoforms. Heterogeneity of alpha-tubulin is concentrated in C-terminal structuraldomain.Synonyms: Alpha-tubulin ubiquitous, Tubulin K-alpha-1, Tubulin alpha-1B chain, Tubulin alpha-ubiquitous chain

    ID gène

    10376

    NCBI Accession

    NP_006073

    UniProt

    P68363

    Pathways

    Dynamique des Microtubules, M Phase
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