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CLS431752

Corning® cell strainer

pore size 100 μm, yellow, sterile, pkg of (individually wrapped), pack of 50 ea

Sinónimos:

Cell strainer

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About This Item

UNSPSC Code:
41104932
NACRES:
NB.24

material

Nylon
yellow

sterility

sterile

packaging

pack of 50 ea
pkg of (individually wrapped)

manufacturer/tradename

Corning 431752

pore size

100 μm

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General description

Corning® 100µm Cell Strainer is a sterile, easy-to-use device for rapidly isolating primary cells to consistently obtain a uniform single-cell suspension from tissues. Applications include stem cells and primary cells. Individually packaged, 50/case.

Application

  • Faster, easier alternative to gauze filtration
  • Ideal for preparation of flow cytometry samples, including:
    Single cell suspensions of blood cells from marrow, pancreas, thymus, tonsil, and lymph nodes
    Stem cells, tissue-derived cells, and cancer cells
    Preparation of specimens for primary cell cultures and immunogens
    Preparation of freezing stocks
    Filtering agglutinative proteins produced in inactivation serum

Features and Benefits

  • Strong nylon mesh with 100- micron pores for optimal performance in a variety of applications
  • Evenly spaced mesh pores providing consistent and reliable results
  • Conveniently accessible in individual packaging
  • Extended lip on strainer enables aseptic handling with forceps
  • Molded color-coded polypropylene frame with tab enables easy handling and identification
  • Fits all major brands of 50mL Conical Tube
  • Disposable, easy-to-use, inexpensive, maintains sample integrity
  • Sterilized by gamma irradiation, noncytotoxic

Legal Information

Corning is a registered trademark of Corning, Inc.

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Epithelial sheet spreading is a fundamental cellular process that must be coordinated with cell division and differentiation to restore tissue integrity. Here we use consecutive serum deprivation and re-stimulation to reconstruct biphasic collective migration and proliferation in cultured sheets of
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American journal of translational research, 12(6), 2379-2395 (2020-07-14)
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Cell, 180(4), 764-779 (2020-02-16)
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