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His Tag antibody

WB, ELISA, IP, IF, FACS Host: Mouse Monoclonal 6G2A9 unconjugated
Catalog No. ABIN387699
  • Target See all His Tag Antibodies
    His Tag
    Reactivity
    Please inquire
    Host
    • 90
    • 60
    • 11
    • 9
    • 5
    • 4
    • 1
    • 1
    Mouse
    Clonality
    • 92
    • 76
    • 10
    Monoclonal
    Conjugate
    • 78
    • 21
    • 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
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This His Tag antibody is un-conjugated
    Application
    • 140
    • 90
    • 38
    • 27
    • 23
    • 17
    • 15
    • 14
    • 14
    • 13
    • 13
    • 7
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    • 1
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    • 1
    Western Blotting (WB), ELISA, Immunoprecipitation (IP), Immunofluorescence (IF), Flow Cytometry (FACS)
    Sequence
    HHHHHH
    Specificity
    THETMHis Tag Antibody, mAb, Mouse recognizes C-terminal, N-terminal, and internal His tagged fusion proteins.
    Characteristics
    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.
    Purification
    Protein A affinity column
    Immunogen
    A synthetic peptide HHHHHH coupled - KLH
    Clone
    6G2A9
    Isotype
    IgG
    Top Product
    Discover our top product His Tag Primary Antibody
  • Application Notes
    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
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Buffer
    PBS, pH 7.4, containing 0.02 % Sodium azide
    Preservative
    Sodium azide
    Precaution of Use
    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.
    Handling Advice
    Avoid repeated freezing and thawing cycles.
    Storage
    4 °C/-20 °C
    Storage Comment
    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).

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    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).

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    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).

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    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 Products
    Target Type
    Tag
    Background
    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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