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BR701330

BRAND® 96-well microplate, U-bottom

round bottom, non-sterile

Synonym(e):

Microplates, Plates, Sample Storage

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About This Item

UNSPSC-Code:
41121800
NACRES:
NB.15
Materialien:
polypropylene
round bottom
Größe:
96 well
Maximales Well-Volumen:
300 μm

Materialien

polypropylene
round bottom

Sterilität

non-sterile

Verpackung

pack of 100 ea

Hersteller/Markenname

BRAND 701330

Größe

96 well

Maximales Well-Volumen

300 μm

Bindungsart

non-treated surface

Allgemeine Beschreibung

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.

Leistungsmerkmale und Vorteile

  • 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.

Rechtliche Hinweise

BRAND is a registered trademark of BRAND GMBH + CO KG

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Julien Racle et al.
Nature biotechnology, 37(11), 1283-1286 (2019-10-16)
Predictions of epitopes presented by class II human leukocyte antigen molecules (HLA-II) have limited accuracy, restricting vaccine and therapy design. Here we combined unbiased mass spectrometry with a motif deconvolution algorithm to profile and analyze a total of 99,265 unique
Timo Strohäker et al.
Nature communications, 10(1), 5535-5535 (2019-12-05)
Parkinson's disease (PD) and Multiple System Atrophy (MSA) are clinically distinctive diseases that feature a common neuropathological hallmark of aggregated α-synuclein. Little is known about how differences in α-synuclein aggregate structure affect disease phenotype. Here, we amplified α-synuclein aggregates from PD
Mateusz Maciejczyk et al.
Oxidative medicine and cellular longevity, 2019, 4393460-4393460 (2019-12-31)
Despite the proven role of oxidative stress in numerous systemic diseases and in the process of aging, little is still known about the salivary redox balance of healthy children, adults, and the elderly. Our study was the first to assess
Lisa-Marie Mauracher et al.
Journal of clinical medicine, 8(10) (2019-10-05)
The exact contribution of neutrophils to post-resuscitative brain damage is unknown. We aimed to investigate whether neutrophil extracellular trap (NET) formation in the early phase after return of spontaneous circulation (ROSC) may be associated with poor 30 day neurologic function
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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