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BR701330

BRAND® 96-well microplate, U-bottom

round bottom, non-sterile

Synonyme(s) :

Microplates, Plates, Sample Storage

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A propos de cet article

NACRES:
NB.15
UNSPSC Code:
41121800
Material:
polypropylene , round bottom
Size:
96 wells
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material

polypropylene , round bottom

sterility

non-sterile

packaging

pack of 100 ea

manufacturer/tradename

BRAND 701330

size

96 wells

well maximum volume

300 μm

suitability

suitable for (bacteriological assays)

binding type

non-treated surface

General description

PP. For volumes up to 300 µl. Compatible with virtually all leading microplate centrifuges. Raised rings around the orifice of each well minimize possible cross-contamination. The plates can be sealed using self-adhesive films, such as DMSO-resistant sealing film (cross-cut) with alphanumeric coding.

Features and Benefits

  • BRAND® 96-well microplate, U-bottom is a deep-well plate ideal for agglutination and other assays requiring stirring and washing of samples.
  • Features a round-shaped well bottom with no edges.
  • Raised rings around the orifice prevent possible cross-contamination.
  • Compatible with a range of microplate centrifuges.
  • Securely sealable with suitable sealing mats or self-adhesive sealing films.
  • Alphanumeric code for accurate identification.
  • Made from high-transparency medical grade polypropylene (PP) that facilitates sample visibility.
  • Chemically resistant to most solvents including DMSO, phenol, and chloroform.

Legal Information

BRAND is a registered trademark of BRAND GMBH + CO KG

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SeongJun Han et al.
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Regulatory T cells are integral to the regulation of autoimmune and anti-tumor immune responses. However, several studies have suggested that changes in T cell signaling networks can result in T cells that are resistant to the suppressive effects of regulatory
Stephen D Carter et al.
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Gefei Chen et al.
Communications biology, 3(1), 32-32 (2020-01-22)
Molecular chaperones play important roles in preventing protein misfolding and its potentially harmful consequences. Deterioration of molecular chaperone systems upon ageing are thought to underlie age-related neurodegenerative diseases, and augmenting their activities could have therapeutic potential. The dementia relevant domain
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