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51153

LUCY® Starter Kit

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About This Item

UNSPSC Code:
12352200
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storage temp.

2-8°C

Application

The LUCY Starter Kit contains three fluorescent protein stains for SDS-PAGE gels.
  • LUCY 506 for high sensitivity staining with a detection limit of 3 ng protein per band. Staining is complete after 60 minutes and detection is possible immediately thereafter.
  • LUCY 565 is recommended for staining SDS-PAGE gels prior to Western blot transfer. With traditional staining, 2 separate gels are required and therefore, double the amount of sample is necessary.
  • LUCY 569 is particularly well suited for protein quantitation, displaying a broad, linear, dynamic range between 10–6,000 ng protein per band.

Legal Information

LUCY is a registered trademark of Sigma-Aldrich Co. LLC

Kit Components Only

Product No.
Description
  • LUCY® 565 solution 50 μL

Kit Components Also Available Separately

Product No.
Description
SDS & Pricing
  • LUCY® 506 solution 50 μL
    SDS
  • LUCY® 569 solution 50 μL
    SDS

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 3 - Repr. 1B

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCBP1551V
BCBN5083V
BCBH7340V
BCBB1545
1436044

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Biji T Kurien et al.
Methods in molecular biology (Clifton, N.J.), 869, 403-405 (2012-05-16)
Gel electrophoresis is an important methodology employed for protein analysis. It is often necessary to elute and recover proteins separated by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). The procedure involves localizing the protein of interest on the gel following
Yi Hu et al.
Molecular biotechnology, 28(1), 63-76 (2004-10-01)
This review focuses on recent developments in gel-based proteomics techniques. By combining traditional sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and two-dimensional gel electrophoretic techniques with recent advances in protein labeling using different classes of molecules (i.e., fluorescent dyes, chemical probes