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生物素-11-dATP

生物素-11-dATP,Biotin-11-dCTP,Biotin-X-5-Propargylamino-dCTP,生物素-X-5-炔丙胺基-dCTP,γ-[N-(Biotin-6-amino-hexanoyl)]-5-propargylamino-2'-deoxycytidine-5'-triphosphate, Triethylammonium salt,γ-[N-(生物素-6-氨基己酰基)]-5-丙炔氨基-2'-脱氧胞苷-5'-三磷酸三乙铵盐。更多视频请关注视频号【艾维缔】。哔哩哔哩【IVDSHOW】。抖音【军哥聊表观】。


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生物素-11-dATP


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目录号

NU1175BIOX

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  • For research use only.
    Please centrifuge briefly before opening (volume ≤2 ml).

    Description:
    Biotin-11-dATP is enzymatically incorporated into DNA/cDNA as substitute for its natural counterpart dATP. The resulting Biotin-labeled DNA/cDNA probes are subsequently detected using streptavidin conjugated with horseradish peroxidase (HRP), alkaline phosphatase (AP), a fluorescent dye or agarose/magnetic beads. Optimal substrate properties and thus labeling efficiency as well as an efficient detection of the Biotin moiety is ensured by a 11-atom linker attached to the 7-Deaza position of adenine.

    Recommended Biotin-16-dATP/dATP ratio for PCR: 50% Biotin-16-dATP/ 50% dATP

    Please note: The optimal final concentration of Biotin-11-dATP may very depending on the application and assay conditions. For optimal produdct yields and high incorporation rates an individual optimization of the Biotin-11-dATP/dATP ratio is recommended.

    Shipping: shipped on gel packs

    Storage Conditions: store at -20 °C
    Short term exposure (up to 1 week cumulative) to ambient temperature possible.

    Shelf Life: 12 months after date of delivery

    Molecular Formula: C30H45N8O15P3S (free acid)

    Molecular Weight: 882.71 g/mol (free acid)

    Exact Mass: 882.19 g/mol (free acid)

    Purity: ≥ 95 % (HPLC)

    Form: filtered solution (30 kDa) in 10 mM Tris-HCl

    Color: colorless to slightly yellow

    Concentration: 1.0 mM - 1.1 mM

    pH: 7.5 ±0.5

    Spectroscopic Properties: λmax 280 nm, ε 12.7 L mmol-1 cm-1 (Tris-HCl pH 7.5)

    Applications:
    Incorporation into DNA/cDNA by
    - PCR with Taq polymerase [1] & in-house data
    - Nick Translation with DNAse I/ DNA Polymerase I [2]
    - Primer Extension with Klenow exo- [3,4]
    - Reverse Transcription with MMLV Reverse Transcriptase [5]

    Selected References:
    [1] Zammatteo et al. (2005) Unambiguous identification of the expressed MAGE-A genes on a DNA microarray. Clin. Chem. 51 (12):2420.
    [2] Dauwerse et al. (1999) Two-colour FISH detection of the inv (16) in interphase nuclei of patients with acute myeloid leukaemia. Br. J. Haematol. 106 (1):111.
    [3] Vorwerk et al. (2008) Microfluidic-based enzymatic on-chip labeling of miRNAs. N. Biotechnol. 25 (2):142.
    [4] Beier et al. (2008) Microfluidic primer extension assay. Methods Mol Biol 822:143.
    [5] Vankoningsloo et al. (2008) Gene expression silencing with 'specific' small interfering RNA goes beyond specificity - a study of key parameters to take into account in the onset of small interfering RNA off-target effects. FEBS J. 275 (11):2738.

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    生物素-11-dCTP

    NU1175BIOX-01 10μL(1mM) 2-8°C

    生物素-11-dCTP

    NU1175BIOX-02 50μL(1mM) 2-8°C
    操作手册 1 1 常温
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    NU1175BIO1X-生物素-11-dATP相关说明

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  • FAQ

     

  • Stage-specific epigenetic priming amplifies gene activation during lineage commitment.

    Arion Foertsch, Naama Hirsch, ..., Asifa Akhtar

    Science Advances  |  2026 Mar 27  |  41894493 

    STAG2 mutations reshape the cohesin-structured spatial chromatin architecture to drive gene regulation in acute myeloid leukemia.

    Alexander Fischer, Benjamín Hernández-Rodríguez, ..., Claudia Gebhard

    Cell Reports  |  2024 Jul 25  |  39084219 

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