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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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About This Item

Code UNSPSC :
41121800
Nomenclature NACRES :
NB.15

Matériaux

polypropylene
round bottom

Stérilité

non-sterile

Conditionnement

pack of 100 ea

Fabricant/nom de marque

BRAND 701330

Taille

96 well

Volume maximum des puits

300 μm

Type de liaison

non-treated surface

Description générale

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.

Caractéristiques et avantages

  • 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.

Informations légales

BRAND is a registered trademark of BRAND GMBH + CO KG

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

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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