Skip to Content
Merck

27813

Coomassie protein assay reagent

Sign In to View Organizational & Contract Pricing.

Select a Size

All Photos(2)

About This Item

NACRES:
NA.21
PubChem Substance ID:
57648233
UNSPSC Code:
12171500
MDL number:
MFCD00163371

InChI

1S/C47H49N3O7S2.Na/c1-6-49(31-35-11-9-13-43(29-35)58(51,52)53)40-21-25-45(33(4)27-40)47(37-15-17-38(18-16-37)48-39-19-23-42(24-20-39)57-8-3)46-26-22-41(28-34(46)5)50(7-2)32-36-12-10-14-44(30-36)59(54,55)56;/h9-30H,6-8,31-32H2,1-5H3,(H2,51,52,53,54,55,56);/q;+1/p-1

SMILES string

[Na+].CCOc1ccc(Nc2ccc(cc2)C(\c3ccc(cc3C)N(CC)Cc4cccc(c4)S([O-])(=O)=O)=C5/C=CC(\C=C5C)=[N+](\CC)Cc6cccc(c6)S([O-])(=O)=O)cc1

InChI key

RWVGQQGBQSJDQV-UHFFFAOYSA-M

form

liquid

density

~1.31 g/mL at 20 °C

storage temp.

2-8°C

Quality Level

200

Related Categories

Application

Suitable for the determination of protein according to Bradford. Five-fold concentrate for tests in microtiter plates; ten-fold concentrate for tests in photometric cuvettes (d=1cm); dilute with H2O

General description

Coomassie protein assay reagent is a protein analysis reagent used for the determination of total protein concentration. The Coomassie dye in the Coomassie (Bradford) reagent binds to protein in the sample leading to an immediate shift in absorption with a concomitant color change of the solution from red to blue. This spectrophotometric measurement of the intensity of this resulting blue color is used to determine the concentration of protein in solutions.

Legal Information

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1 - Skin Corr. 1B - STOT SE 1

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

109.4 °F

flash_point_c

43 °C

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000500160
0000500159
0000500159
0000500160
0000458898

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Diwakar Dahal et al.
Plant molecular biology, 73(6), 643-658 (2010-05-25)
Proteomics approach was used to elucidate the molecular interactions taking place at the stem cell wall level when tomato species were inoculated with Ralstonia solanacearum, a causative agent of bacterial wilt. Cell wall proteins from both resistant and susceptible plants
An-Cheng Huang et al.
Oncology letters, 19(3), 2397-2403 (2020-03-21)
Furoquinolone and its derivatives exhibit antimicrobial, anti-allergic, anti-inflammatory and anticancer properties. The present study investigated the anti-tumor activity of synthesized intermediates of furoquinolone in human promyelocytic leukemia HL-60 cells. The biological effects of the active compound ethyl 2-anilino-4-oxo-4,5-dihydrofuran-3-carboxylate (compound 131)
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.
M M Bradford
Analytical biochemistry, 72, 248-254 (1976-05-07)

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