Skip to Content
Merck
All Photos(1)

Key Documents

More Documents

Safety Information

APPA002

Sigma-Aldrich

Green Universal Detection Reagent

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

UNSPSC Code:
12352204
NACRES:
NA.25

form

solution

Quality Level

200

technique(s)

microbe id | specific enzyme detection: suitable

shipped in

dry ice

storage temp.

−20°C

General description

GreenUniversal Detection Reagent is formulated with green fluorescent protein (GFP),which is a part of the split fluorescent protein (FP) system that may be usedto quantify the expression level of a tagged protein of interest (POI).

Application

The S1-10 Universal Detection Reagent is provided as a ready-to-use solution for use with the In Vitro "Fold ′n′ Glow" Solubility Assay Kits:

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

APPA002-20ML-PW:
APPA002-VAR:
APPA002-20ML-LBL:
APPA002-BULK:
APPA002-20ML:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

G S Waldo et al.
Nature biotechnology, 17(7), 691-695 (1999-07-15)
Formation of the chromophore of green fluorescent protein (GFP) depends on the correct folding of the protein. We constructed a "folding reporter" vector, in which a test protein is expressed as an N-terminal fusion with GFP. Using a test panel
Stéphanie Cabantous et al.
Nature biotechnology, 23(1), 102-107 (2004-12-08)
Existing protein tagging and detection methods are powerful but have drawbacks. Split protein tags can perturb protein solubility or may not work in living cells. Green fluorescent protein (GFP) fusions can misfold or exhibit altered processing. Fluorogenic biarsenical FLaSH or

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service