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Proteinase K (liquida) HC4502A Image Featured
  • Proteinase K (liquida) HC4502A

Dapibus K (Liquid)


Cat No: HC4502A

Sarcina: 5ml/100ml/1L/10L

Free of DNase, RNase, Nickase

Actio: ≥800 U/ml

Vita III annis fasciae

One-batch facultatem 1500L (30kg)

 

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Product detail

Data

Cat No: HC4502A

Proteinase K est protease stabilis serine cum specificitate latis substratis.Multos servo in re publica depravat etiam coram detergents.Ex crystallo et hypothetica structurae testimonia enzyme indicat, ad subtilisin familiam cum activo catalytico trias (Asp.39-His69- Ser224).Praedominans situs bipertitis est vinculum peptidis adhaerens globi carboxyli amino acidi aliphatici et aromatici cum coetibus alpha amino inclusis.Vulgo pro lataproprietatem.


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  • Specification

    Aspectus

    Hyalina ut lux brunneis liquor

    Actio

    ≥800 U/ml

    Dapibus concentration

    ≥20 mg/ml

    DNase

    Nihil detectum

    RNase

    Nihil detectum

     

    Repono Conditions

    Condite ad temperies 2-8℃.

     

    Properties

    EC numerus

    3.4.21.64 (Recombinante ex Tritirachium album)

    M. pondus

    29 kDa (SDS-PAGE)

    Isoelectric punctum

    7.81

    optimum pH

    7.0-12.0 Fig.1

    Optimum temperatus

    65 Fig.2

    PH stabilitas

    pH 4.5-12.5 (25℃, 16 h) Fig

    Scelerisque status

    Infra 50℃ (pH 8.0, 30 min) Fig

    Activators

    SDS, urea

    Inhibitors

    Diisopropyl fluorophosphate;phenylmethylsulfonyl fluoride

     

    Applications

    1. Diagnostic ornamentum geneticae

    2. RNA et DNA extraction kits

    3. Extractio partium non- interdum e textuum, degradatione immunditiarum interdum, ut DNA vaccina et praeparatio heparin.

    4. Praeparatio chromosomatis DNA ab electrophoresi pulsante

    5. Occidentis opprobrium

    6. Enzymatica glycosylata albumin reagentia in vitro diagnosi

     

    Cautiones

    Gerunt chirothecas tutelares et goggles cum utendo vel appendendo, et post usum bene ventilatas.Productum hoc facere potest cutis reactionem allergic et gravem oculi irritationem.Si haustus, allergiam vel asthma signa vel dyspnoeam causare potest.Sit irritatio respiratorii causa.

     

    Assay

    Unitas definition

    Unitas una (U) definitur quantum enzyme ad hydrolyzi casein requiritur ad 1 μmol tyrosinum per minutum producendum sub his conditionibus.

     

    Reagentia praeparatio

    Reagens I: 1g casein lac in 50ml 0.1M sodium solutionis phosphatae (pH 8.0), incubatis 65-70 aqua per 15 min, excitatum et dissolutum, ab aqua refrigeratum, a sodio hydroxide ad pH8.0 accommodatum, fixit. volumen 100ml.

    Reagens II: Solutio TCA: 0.1M acidum trichloroaceticum, 0.2M sodium acetatis, 0.3M acidum aceticum.

    Reagent III: 0.4M Na2CO3solutio.

    Reagent IV: Forint iodi aqua pura dilutum 5 temporibus.

    Reagens V: Enzyme diluens: 0.1M solutio phosphatae sodium (pH 8.0).

    Reagent VI: Solutio Tyrosina: 0, 0.005, 0.025, 0.05, 0.075, 0.1, 0.25 umol/ml tyrosina dissoluta cum 0.2M HCl.

     

    De modo procedendi

    1. 0,5ml reagentia I prae-calefactum ad 37℃, 0,5ml solutionis enzyme adde, bene misce, et incubant 37℃ pro 10min.

    2. Adde 1ml reagentes II ad resistendum reactionem, miscere bene, et pergere incubationem pro 30min.

    3. solutio reactionis centrifugae.

    4. Accipe 0.5ml supernatantem, adde 2.5ml reagens III, 0.5ml reagens IV, misce bene et incubare 37℃ pro 30min.

    5. OD660determinari ad OD1;blank control group: 0.5ml reagens V adhibetur ad solutionem enzyme reponere ad determinare OD660ut OD2, OD=OD1-OD2.

    6. L-tyrosinum vexillum curvae: 0.5mL solutionem tyrosinam diversam intentionem L, 2.5mL Reagenti III, 0.5mL Reagenti IV in 5mL tubi centrifugii, incubare 37℃ pro 30min, deprehendere pro OD660ob diversam intentionem L-tyrosinam, tum curvae regulae Y=kX+b consecuta, ubi Y est L-tyrosina concentratio, X est OD.600.

     

     Calculus

     

    2: Totalis voluminis solutionis reactionis (ml)

    0.5: Volume enzyme solutionis (mL)

    0,5: Reactio liquida volumen in determinatione chromogenic (mL)

    X: Reactio tempus (min)

    Df: Dilutio multiplex

    C: Enzyme concentration (mg/mL)

     

    References

    1. Wieger U & Hilz H. FEBS Lect.(1972);23:77.

    2. Wieger U & Hilz H. Biochem.Biophys.Res.Communi.(1971);44:513.

    3. Hilz, H.et al.EUR.J. Biochem.(1975);56: 103-108.

    4. Sambrook Jet al. Molecular Cloning: A Laboratory Manuale, 2nd edition, Frigidum Spring Harbour Laboratory Press, Frigidum Spring Harbour (1989).

     

    Figurae

    Fig. 1 Optimum pH

    100mM solutio quiddam: pH6.0-8.0, Na-phosphas;pH8.0- 9.0, Tris-HCl;pH9.0-12.5, Glycine-NaOH.Enzyme concentration:1mg/mL

     

    Fig

    Reactio in 20mM K-phosphate quiddam pH 8.0.Enzyme concentration: 1mg/mL

     

    Fig Stabilitas

    25℃, 16 h-tractatio cum 50mM solutionis quiddam: pH 4.5-5.5, acetate;pH 6.0-8.0, Na-phosphate;pH 8.0-9.0, Tris-.HCl.pH 9.0-12.5, Glycine-NaOH.Enzyme concentration: 1mg/mL

     

    Fig stabilitas

    30 min-tractatio cum 50mM Tris-HCl quiddam, pH 8.0.Enzyme concentration: 1mg/mL

     

    Fig stabilisty at 25℃

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