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Viresolve 180 Process Area Mod

ule (20-stack) Protein Purification
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  • 询价
  • VPVH20CN1
  • 2025年07月12日
  • Protein Purification
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 应用范围

      Protein Purification

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      大量

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    Description:
    Viresolve 180 Process Area Module (20-stack)
    Trade Name:
    Viresolve
    Key Applications:
    Protein Purification
    Operating Temperature Range, °C:
    4–37
    Hold-up Volume, mL:
    1410
    Length, cm (in):
    38.6 (15.2)
    Filter Material:
    Hydrophilic PVDF
    pH Range:
    4–8
    Maximum Inlet Pressure, bar (psi):
    0.35 (5) @ 4–37 °C
    Filtration Area, m2 :
    1.38
    Weight, kg (lb):
    6.4 (14.1)
    Height, cm (in):
    9.9 (3.88)
    Viral Clearance Device Type:
    TFF Filters
    Width, cm (in):
    19.4 (7.6)
    Sterilization:
    Not autoclavable or steam-sterilizable
    Filter Code:
    VPVH
    Max Transmembrane Pressure, bar (psig):
    0.35 (5) @ 4–37 °C
    Gravimetric Extractables:
    ≤200 mg after 24-h soak in water
    Permeate Flow Rate Range, mL/min:
    200–1500
    Device Material:
    PVDF
    CorrTest:
    ≥ 1.1 @ 1030 mbar (15 psig)

    Product Family Information

    Viresolve Process Area Modules

    Viresolve process area modules are self-contained, single-use disposable modules designed to remove viruses from protein solutions at process scale. Viresolve modules are fabricated from a single material of construction, polyvinylidene fluoride (PVDF). Each unit is 100% integrity tested during manufacturing by CorrTest to assure integrity.

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    更多产品技术资讯,请访问密理博中国博客:http://blog.milliporechina.com

    详细描述见链接:http://www.millipore.com/catalogue/item/VPVH20CN1

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    图标文献和实验
    相关实验
    • Purification of Antiserum or Ascites by Protein A/G Chromatography

      in case the antibody was eluted.Ⅳ After washing the column, collect a 20 microliter fraction and test for protein by adding it to 180 microliters of Coomassie Blue reagent to test for protein. If the sample turns blue, wash the column with an additional 50

    • Purification

      cfuge at top speed. Transfer supernatant to polyallomer tubes and centrifuge 1.5 hr at 27,000 rpm at 4' in SW 28.1 rotor (have to divide into 3 tubes). (See also alternate procedure.)   C. Resuspend phage pellet in 180 141 5OmM Tris, ph

    • Purification of DNA from lambda phage

      tube,extract with phenol again.You can do a third phenol extraction if there is still a lot of white denatured protein at the interface. E.Add 200 III CHCOC3,shake,microcentrifuge briefly.Transfer aqueous layer to new tube,repeat. F.Add 20 jil of 3M

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