Thermo Scientific™ Pierce Nickel Coated Plates provide a simple format to bind His-tagged fusion proteins for ELISA and other plate-based assays involving protein interactions of expressed recombinant proteins.
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Catalog Number
Color
Format
Detection Method
15242
White
Standard
Chemiluminescence
15342
Black
Standard
Fluorescence
15142
Clear
Strip Plate
Colorimetric
15442
Clear
Standard
Colorimetric
4 Options
Catalog number 15242
Price (CNY)
4,600.00
Each
Add to cart
Color:
White
Format:
Standard
Detection Method:
Chemiluminescence
Request bulk or custom format
Price (CNY)
4,600.00
Each
Add to cart
These Ni(2+) chelate-coated plates are ideal for analyzing polyhistidine-tagged fusion proteins by ELISA-based methods. Proteins that contain a succession of several histidine residues at the amino or carboxyl terminus have a strong binding affinity for metal. Bacterial lysates containing polyhistidine-tagged fusion proteins can be added directly to the plates without the need for blocking. The clear, white or black plates can be used with colorimetric, chemiluminescent or fluorescent detection methods, respectively.
Thermo Scientific Pierce Nickel Coated White 96-Well Plates provide a simple format to bind His-tagged fusion proteins for ELISA and other plate-based assays involving protein interactions of expressed recombinant proteins. These white plates can be used with chemiluminescent detection methods.
Features of Pierce Nickel Coated Plates include: • Ni2+ activated surface enables metal-chelate binding of His-tagged proteins • Detergents used to lyse cells don't inhibit binding to activated plates as they do with plain polystyrene • Better binding for sensitive assays compared to other commercially available nickel-activated plates • Detection limit: 1 ng of polyhistidine fusion protein • Binding capacity: approx. 9 pmol His-tagged protein (27 kDa) per well • Activation level: 200 μL
These Ni(2+) chelate-coated plates are ideal for analyzing polyhistidine-tagged fusion proteins by ELISA-based methods. Proteins that contain a succession of several histidine residues at the amino or carboxyl terminus have a strong binding affinity for metal. Bacterial lysates containing polyhistidine-tagged fusion proteins can be added directly to the plates without the need for blocking.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Binding PropertyStandard Capacity, Affinity
Detection MethodChemiluminescence
Packaging5 Plates
Plate BlockingBlocker™ BSA Buffer
Product TypeMicroplate
Quantity5 plates
ColorWhite
FormatStandard
MaterialPolystyrene
No. of Wells96
Product LinePierce
Surface TreatmentDivalent Nickel, Metal Chelate
Volume (Metric) Well200 μL
Unit SizeEach
Contents & Storage
Upon receipt store plates at 4°C in unopened pouches. Once opened, place unused plates in a resealable bag with desiccant and store at 4°C.
Frequently asked questions (FAQs)
What is the binding capacity for Pierce Nickel Coated Plates?
The binding capacity for Pierce Nickel Coated Plate is approximately 9 pmol His-tagged protein (27 kDa) per well.
Why should I use ultra-pure water for washing Pierce Nickel Coated Plates?
The water used for washing of microplates as well as all assay reagents, must be of absolutely ultra-pure quality. This means that no metal ions should be present in the water, as this will bind to the His-tag and thereby decrease the binding of the fusion protein to the nickel-chelate complex.
Is it possible to elute the bound His-tagged fusion protein/peptide from the surface of Pierce Nickel Coated Plates?
Yes. For instance, use imidazole in concentrations >500 mM in Tris at pH 7.5 or a high concentration of EDTA.
With Pierce Nickel Coated Plates, can any reagent interfere with the binding between the nickel-chelate complex and the His-tagged fusion biomolecule?
Ionic detergents (e.g., SDS) will interfere with the binding as well as high concentrations of chelating reagents like EDTA, EGTA, and very strong electron donors like metal ions.
Can I use Pierce Nickel Coated Plates to measure the amount of bound His-tagged fusion protein/peptide?
To determine the approximate amount of bound His-tagged fusion protein/peptide, a standard curve of a previously purified preparation can be applied.