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His Tag Antikörper

WB, ELISA, IP, IF, FACS Wirt: Maus Monoclonal 6G2A9 unconjugated
Produktnummer ABIN387699
  • Target Alle His Tag Antikörper anzeigen
    His Tag
    Reaktivität
    Bitte anfragen
    Wirt
    • 89
    • 60
    • 11
    • 9
    • 5
    • 4
    • 1
    • 1
    Maus
    Klonalität
    • 91
    • 76
    • 10
    Monoklonal
    Konjugat
    • 76
    • 22
    • 13
    • 13
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
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    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser His Tag Antikörper ist unkonjugiert
    Applikation
    • 138
    • 88
    • 36
    • 25
    • 24
    • 15
    • 14
    • 14
    • 13
    • 13
    • 13
    • 7
    • 7
    • 5
    • 5
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunoprecipitation (IP), Immunofluorescence (IF), Flow Cytometry (FACS)
    Sequenz
    HHHHHH
    Spezifität
    THETMHis Tag Antibody, mAb, Mouse recognizes C-terminal, N-terminal, and internal His tagged fusion proteins.
    Produktmerkmale
    Anti-His mAb is produced from mice ascites and purified by protein A affinity column. This antibody recognizes native as well as denatured forms of synthetic polyhistidine and polyhistidine-tagged fusion proteins. The product reacts with fusion proteins expressed in bacteria, insect cells, and mammalian cells. Anti-His mAb recognizes His tags placed at N-terminal, C-terminal, and internal regions of fusion proteins. Anti-His mAb can be used in Western blot analyses, Dot blot analyses, ELISA, immunofluorescent staining, and flow cytometry of cultured cells.
    Aufreinigung
    Protein A affinity column
    Immunogen
    A synthetic peptide HHHHHH coupled - KLH
    Klon
    6G2A9
    Isotyp
    IgG
    Top Product
    Discover our top product His Tag Primärantikörper
  • Applikationshinweise
    Working concentrations for specific applications should be determined by the investigator. The appropriate concentrations may be affected by secondary antibody affinity, antigen concentration, the sensitivity of the method of detection, temperature, the length of the incubations, and other factors. The suitability of this antibody for applications other than those listed below has not been determined. The following concentration ranges are recommended starting points for this product.
    ELISA: 0.05-0.2 µg/mL
    Western blot: 0.1-0.2 µg/mL
    Immunoprecipitation (IP): 1 µg/mL
    Immunofluorescent staining: 1 µg/mL
    Flow cytometry: 1 µg/mL
    Other applications: user-optimized
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Buffer
    PBS, pH 7.4, containing 0.02 % Sodium azide
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    WARNING: Reagents contain sodium azide. Sodium azide is very toxic if ingested or inhaled. Avoid contact with skin, eyes, or clothing. Wear eye or face protection when handling. If skin or eye contact occurs, wash with copious amounts of water. If ingested or inhaled, contact a physician immediately. Sodium azide yields toxic hydrazoic acid under acidic conditions. Dilute azide-containing compounds in running water before discarding to avoid accumulation of potentially explosive deposits in lead or copper plumbing.
    Handhabung
    Avoid repeated freezing and thawing cycles.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    The antibody is stable in lyophilized form if stored at -20°C or below. The reconstituted antibody can be stored for 2-3 weeks at 2-8°C. For long term storage, aliquot and store at -20°C or below.
  • Kaufmann, Brangsch, Kader, Saatz, Mangarova, Zacharias, Kempf, Schwaar, Ponader, Adams, Möckel, Botnar, Taupitz, Mägdefessel, Traub, Hamm, Weller, Makowski: "ADAMTS4-specific MR probe to assess aortic aneurysms in vivo using synthetic peptide libraries." in: Nature communications, Vol. 13, Issue 1, pp. 2867, (2022) (PubMed).

    Dupont-Deshorgue, Oudart, Brassart, Deslee, Perotin, Diebold, Monboisse, Ramont, Brassart-Pasco: "A competitive enzyme-linked immunosorbent assay for quantification of tetrastatin in body fluids and tumor extracts." in: Analytical biochemistry, Vol. 482, pp. 16-21, (2015) (PubMed).

    Locke, Toth, Petroski: "Lys11- and Lys48-linked ubiquitin chains interact with p97 during endoplasmic-reticulum-associated degradation." in: The Biochemical journal, Vol. 459, Issue 1, pp. 205-16, (2014) (PubMed).

    Kitevska, Roberts, Pantaki-Eimany, Boyd, Scott, Hawkins: "Analysis of the minimal specificity of caspase-2 and identification of Ac-VDTTD-AFC as a caspase-2-selective peptide substrate." in: Bioscience reports, (2014) (PubMed).

    Duquesne, Bozonnet, Bordes, Dumon, Nicaud, Marty: "Construction of a highly active xylanase displaying oleaginous yeast: comparison of anchoring systems." in: PLoS ONE, Vol. 9, Issue 4, pp. e95128, (2014) (PubMed).

    Farrow, Rachakonda, Gu, Krendelchtchikova, Nde, Pratap, Lima, Villalta, Matthews: "Immunization with Hexon modified adenoviral vectors integrated with gp83 epitope provides protection against Trypanosoma cruzi infection." in: PLoS neglected tropical diseases, Vol. 8, Issue 8, pp. e3089, (2014) (PubMed).

    Han, Vitre, Fachinetti, Cleveland: "Bimodal activation of BubR1 by Bub3 sustains mitotic checkpoint signaling." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 111, Issue 40, pp. E4185-93, (2014) (PubMed).

    Chen, Taylor, Fowler, Galan, Wang, Wolin: "An RNA degradation machine sculpted by Ro autoantigen and noncoding RNA." in: Cell, Vol. 153, Issue 1, pp. 166-77, (2013) (PubMed).

    West, Dupré, Yu, Paton, Miedzinska, McNeilly, Davis, Burt, Loudon: "Npas4 is activated by melatonin, and drives the clock gene Cry1 in the ovine pars tuberalis." in: Molecular endocrinology (Baltimore, Md.), Vol. 27, Issue 6, pp. 979-89, (2013) (PubMed).

    Stenner, Liewen, Göttig, Henschler, Markuly, Kleber, Faust, Mischo, Bauer, Zweifel, Knuth, Renner, Wadle: "RP1 is a phosphorylation target of CK2 and is involved in cell adhesion." in: PLoS ONE, Vol. 8, Issue 7, pp. e67595, (2013) (PubMed).

    Son, Shen, Margueron, Reinberg: "Nucleosome-binding activities within JARID2 and EZH1 regulate the function of PRC2 on chromatin." in: Genes & development, Vol. 27, Issue 24, pp. 2663-77, (2013) (PubMed).

    Guler, Liu, Vaithiyalingam, Arnett, Kremmer, Chazin, Fanning: "Human DNA helicase B (HDHB) binds to replication protein A and facilitates cellular recovery from replication stress." in: The Journal of biological chemistry, Vol. 287, Issue 9, pp. 6469-81, (2012) (PubMed).

    Rubio-Infante, Govea-Alonso, Alpuche-Solís, García-Hernández, Soria-Guerra, Paz-Maldonado, Ilhuicatzi-Alvarado, Varona-Santos, Verdn-Terán, Korban, Moreno-Fierros, Rosales-Mendoza: "A chloroplast-derived C4V3 polypeptide from the human immunodeficiency virus (HIV) is orally immunogenic in mice." in: Plant molecular biology, Vol. 78, Issue 4-5, pp. 337-49, (2012) (PubMed).

    Amparyup, Sutthangkul, Charoensapsri, Tassanakajon: "Pattern recognition protein binds to lipopolysaccharide and ?-1,3-glucan and activates shrimp prophenoloxidase system." in: The Journal of biological chemistry, Vol. 287, Issue 13, pp. 10060-9, (2012) (PubMed).

    Horstman, Darwin: "Phage shock proteins B and C prevent lethal cytoplasmic membrane permeability in Yersinia enterocolitica." in: Molecular microbiology, Vol. 85, Issue 3, pp. 445-60, (2012) (PubMed).

    Qian, Zhu, Li, Belevych, Chen, Zhao, Herness, Quan: "Interleukin-1R3 mediates interleukin-1-induced potassium current increase through fast activation of Akt kinase." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 109, Issue 30, pp. 12189-94, (2012) (PubMed).

    Wang, Zhao, Sun, Liu, Weng: "Enhancing catalytic activity of a hybrid xylanase through single substitution of Leu to Pro near the active site." in: World journal of microbiology & biotechnology, Vol. 28, Issue 3, pp. 929-35, (2012) (PubMed).

    Frank, McDonald, Karata, Huston, Woodgate: "A strategy for the expression of recombinant proteins traditionally hard to purify." in: Analytical biochemistry, Vol. 429, Issue 2, pp. 132-9, (2012) (PubMed).

    Reitter, Mills: "Canonical protein splicing of a class 1 intein that has a class 3 noncanonical sequence motif." in: Journal of bacteriology, Vol. 193, Issue 4, pp. 994-7, (2011) (PubMed).

    Chatfield, Mulhern, Burnside, Cianciotto: "Legionella pneumophila LbtU acts as a novel, TonB-independent receptor for the legiobactin siderophore." in: Journal of bacteriology, Vol. 193, Issue 7, pp. 1563-75, (2011) (PubMed).

  • Target
    His Tag
    Abstract
    His Tag Produkte
    Substanzklasse
    Tag
    Hintergrund
    Monoclonal antibodies specific to six histidine tags can greatly improve the effectiveness of several different kinds of immunoassays, helping researchers identify, detect, and purify polyhistidine fusion proteins in bacteria, insect cells, and mammalian cells. However, since 6XHis-tag is poorly immunogenic, it needs to be conjugated to KLH or some other carrier as an immunogen. After hundreds of selection cycles, researchers at successfully isolated an antibody against His-tag. Anti-His mAb (subtype IgG1) has very high affinity. Tests performed at show that the antibody can also recognize 4xHis- and 5xHis-tags. This means that even if the 6xHis-tag is only partially exposed, it will still be recognized and bound by this antibody.
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