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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

Le tarif et la disponibilité ne sont pas disponibles actuellement.

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

Comparer avec des articles similaires

Voir la comparaison complète

Montrer les différences

1 of 4

Cet article
CLS3365CLS3359BR701354
material

polypropylene , round bottom

material

polypropylene , round bottom clear

material

polypropylene , round bottom clear

material

polypropylene

sterility

non-sterile

sterility

non-sterile

sterility

sterile

sterility

non-sterile

packaging

pack of 100 ea

packaging

bag of 25 ×

packaging

bag of 25 ×

packaging

pack of 24 ea

manufacturer/tradename

BRAND 701330

manufacturer/tradename

Corning 3365

manufacturer/tradename

Corning 3359

manufacturer/tradename

BRAND 701354

well maximum volume

300 μm

well maximum volume

-

well maximum volume

-

well maximum volume

-

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

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Certificats d'analyse (COA)

Lot/Batch Number

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Consulter la Bibliothèque de documents

Stephen D Carter et al.
Science advances, 6(14), eaay9572-eaay9572 (2020-04-10)
The endoplasmic reticulum (ER) is a highly dynamic network of membranes. Here, we combine live-cell microscopy with in situ cryo-electron tomography to directly visualize ER dynamics in several secretory cell types including pancreatic β-cells and neurons under near-native conditions. Using
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
SeongJun Han et al.
Oncoimmunology, 9(1), 1737368-1737368 (2020-04-22)
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
D Tews et al.
Redox biology, 26, 101286-101286 (2019-08-06)
Brown adipose tissue (BAT) has been considered beneficial for metabolic health by participating in the regulation of glucose homoeostasis. The browning factors that improve glucose uptake beyond normal levels are still unknown but glucose uptake is not affected in UCP1
Rosalie Heilig et al.
Life science alliance, 3(6) (2020-04-30)
Caspase-1 drives a lytic inflammatory cell death named pyroptosis by cleaving the pore-forming cell death executor gasdermin-D (GSDMD). Gsdmd deficiency, however, only delays cell lysis, indicating that caspase-1 controls alternative cell death pathways. Here, we show that in the absence

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