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CLS3766

Corning® 384孔微孔板，低边

NBS™ (non-binding surface), black polystyrene, non-sterile, lid: no, pack of 25

同義詞:

384 multiwell plates, 384 well immunoassay plates, 384 well microplates, 384 well microtiter plates, 384 well plates, immunoassay plates

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About This Item

分類程式碼代碼:
41121800
NACRES:
NB.24
暫時無法取得訂價和供貨情況

材料

black polystyrene
clear bottom
flat wells
polystyrene

無菌

non-sterile

特點

lid: no
skirt
 plate format: low flange

包裝

case of 100 ea
pack of 25

製造商／商標名

Corning 3766

最大體積

112 μL

尺寸

384 wells

有效容積

80 μL

顏色

black

適合性

suitable for (cell cuture)

結合類型

NBS™ (non-binding surface)

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相關類別

一般說明

Corning® 384-well ELISA Microplates with flat-bottom and low flange are high-quality, high-performance microplates that are widely used for laboratory assays. It improves assay sensitivity and performance.

應用

Corning® 384 well microplate, low flange has been used in enzyme activity assays to perform the phosphatase reactions.[1] It has also been used to perform malachite green ATPase assays.[2]

特點和優勢

  • Black wall plates provide low background fluorescence, minimal light scatter, and reduced crosstalk, ensuring accurate and precise measurements
  • Thermally stable microplates (4°C to 37°C) ensure consistent performance over a wide range of temperature and storage conditions.
  • Chemically stable and noncytotoxic microplates are designed to be compatible with aqueous solutions containing low levels (<20%) of organic solvents, including ethanol and DMSO.
  • Meets SBS microplate standards to ensure compatibility with automated instruments.
  • Suitable for bar coding

法律資訊

Corning is a registered trademark of Corning, Inc.
NBS is a trademark of Corning, Inc.

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CRISPR-associated DinG protein (CasDinG) is essential to type IV-A CRISPR function. Here, we demonstrate that CasDinG from Pseudomonas aeruginosa strain 83 is an ATP-dependent 5'-3' DNA translocase that unwinds double-stranded (ds)DNA and RNA/DNA hybrids. The crystal structure of CasDinG reveals a
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Discovery of protein-binding fragments for precisely defined binding sites is an unmet challenge to date. Herein, formylglycine is investigated as a molecular probe for the sensitive detection of fragments binding to a spatially defined protein site . Formylglycine peptide 3

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