echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Biochemistry News > Biotechnology News > DNA probes mark the preparation of commonly used reagents.

    DNA probes mark the preparation of commonly used reagents.

    • Last Update: 2020-10-26
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    (1) 10 × pan buffer: 200mmol/l Tris-HCl, pH7.4 containing 50mmol /L MgCl2;
    (2) gap translation reaction termination fluid: 200mmol/L NaCl; 10mmol/l Tris-HCl, pH7.4; 11mmol/L
    . EDTA
    ; 0.5%
    SDS
    .
    (3) DNaseI.: Dry powdered DNaseI. (2000 to 3000u/mg) dissolved in 20mmol/l Tris-HCl, pH7.5 (1mg/ml), 10 sl, -20C for one year.
    (4) 10×
    . DNA
    polymerase I. (Klenow fragment) buffer: 500mmol/l Tris-HCl, pH6.6; 100mmol/L Mg-Cl2; 10mmol/L
    DTT
    ; 0.5mg BSA.
    (5)10×
    Kinase
    Buffer: 500mmol/L Tris-HCl, pH7.4, 50mmol/L MgCl2; 20mmol/L DTT; 1.0mmol/L subseminide.
    (6)10× random lead marker buffer; 500mmol/l Tris-HCl, pH6.6; 100mmol/L MgCl2; 10mmol/L β- base ethanol; 500μg/ml BSA.
    (7)1× tail buffer: 100mmol/L potassium dithyl, pH7.0, 1mmol/l CoCl2 0.2mmol/L DTT.
    (8) 1mol/L MgCl2:MgCl2 47.60g dissolved in 500ml water, 100ml split, autocultension, room temperature preservation.
    (9) 0.25mol/L EDTA (Ph8.0): EDTA 52.02g dissolved in 400ml water, pH to 8.0, added water to 500ml, 100ml displodged, autocultension, room temperature preservation.
    (10) 4mol/L sodium acetate: take 82g of aqueous sodium acetate dissolved in 200ml water, pH to 6.5 with acetic acid, add water to 250ml, autocultension, or 0.45 m membrane
    filtration
    , room temperature preservation.
    (11) 10% SDS: 10g SDS (sodium tetranyl sulfate) dissolved in 50 ml of water, added water to 100 ml, stored at room temperature after loading.
    (12)20×SSC: Take NaCl 175.3g; sodium citrate 88.2g; add water to 1000ml, tune pH to 7.0 with 10mol/l NaOH; autocultension, room temperature preservation.
    (13) sterile water: 100ml deionized or double steamed water, divided, autocultension, room temperature preservation, only one week after opening the bottle.
    (14)10× Kinase buffer: 500mmol/L Tris-HCl, pH7.4; 100mmol/L MgCl2; 50mmol/l DTT; 10mmol/L subseminide (not required).
    (15) T4 polymer
    nucleotides
    kinase: 10u/l, stored in glycerin, -20 degrees C.
    (16) TE buffer (Tris/EDTA): Tris, 10mmol/l pH7.4 (0.5ml 2mol/L storage), 1.0mmol/l ED-TA, pH8.0 (20 sl 0.5mol/L) storage, plus water to 100ml, room temperature.
    (17) 2mol/L Tris-HCl pH7.4: Tris242.2g dissolved in 850ml, thickened HCl 75ml, stirring slowly to pH7.4, plus water to 1000ml.
    (18) 1mol/L DTT (dithioneol): 3.0g DTT dissolved in 20 ml of water, divided, stored at -20 degrees C.
    (19) 0.5mol/L EDTA (acetylene diacetate di sodium salt): Add 300ml water to the
    beaver
    , add 93.5g EDTA-Na2.2H2O, mix well, add 10mol/l NaOH to 8.0, add water to 500ml.
    (20) 10mol/L NaOH:200g NaOH dissolved in 450ml water, mixed well, then added water to 500ml.
    (21) 5mol/L NaCl: 292.25g NaCl, plus water to 1000ml.
    (22) 1mol/L HCl: Plus 86.2 ml of hydrochloric acid to 913.8 ml of water.
    (23) 1mol/L CaCl2:147g CaCl2:2H2O, dissolved in 1000ml water, autocultension, room temperature preservation.
    .
    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.