Molecular Biology
FISH Probes:
Revealing the Hidden Stories of Cells, One Molecule at a Time
In Situ Hybridization is a powerful technique that allows you to visualize and analyze specific nucleic acid sequences within cells or tissue sections. To achieve truly groundbreaking results, choosing the right probes is of utmost importance. That's why we have meticulously curated this exceptional collection:
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Description
The NeoPRO 10 Prestained Protein Ladder (NB-59-0002) is a combination of 10 pre-stained proteins with molecular weights ranging from 6.5 to 270 kDa.
The 10 recombinant proteins in the ladder are covalently coupled with a blue chromophore.
The ladder includes 2 orange bands at 30 kDa and 270 kDa, as well as a green band at 52 kDa, which function as reference bands.
It is designed to monitor the size and separation of proteins...
Description
The NeoPRO Western Substrate is a luminol-based enhanced chemiluminescent substrate.
It is sensitive and compatible with conducting immunoblots with horseradish peroxidase (HRP)–conjugated secondary antibodies.
Enables mid-femtogram to high-femtogram detection of antigen.
Offers excellent sensitivity and long signal duration
Allows for digital and film-based imaging without signal loss...
Description
Designed for simple, one-step, and rapid purification of immunoglobulins
Traps proteins through covalent binding to prevent sample loss
Allows capture of broad source species and IgG subclasses
Enables column reusing
Compatible with standard liquid chromatography instruments (including ÄKTA™ FPLC's), peristaltic pumps, and syringes.
Our Products:
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Description
NeoSpin centrifugal filters from Neo Biotech:
Efficient and rapid sample preparation
Polypropylene housing with a polyethersulfone (PES) membrane
High flow rates and high protein retention
Heat-sealed membrane eliminates adhesives and is downstream extractable
Compatible with pH 1 to 9
Enables maximum protein recovery without introducing pipetting errors
Low binding membrane and polypropylene housing for ...
Description
The new generation of Taq-derived DNA polymerases NB-60-0005 optimized for standard PCR applications.
Engineered to produce high DNA yields in shorter PCR running times (15-30 s/kb extension).
Lacks 3´→5´ exonuclease activity and supports reliable amplification of a wide range of DNA templates up to 6 kb.
Suitable for PCR under minimal optimization conditions.
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Description
qPCR Green Master Mix (2x) NB-60-0003-01 is a Defined reaction mixture for real-time PCR.
It is highly efficient and optimized for optimal performance.
The mix includes a hot-start enzyme control mechanism, enhancing detection sensitivity.
Incorporates the latest advancements in PCR enhancer technology, such as buffer chemistry and robustly engineered enzymes.
Engineered to deliver precise and dependable results for accurate analysis...
Description
NeoProof DNA polymerase NB-60-0006 : a recombinant enzyme with high fidelity and excellent PCR performance.
Includes 3´→5´ exonuclease proofreading for improved accuracy.
Efficiently amplifies longer PCR products (≤10 kb) and enables site-directed mutagenesis.
Recommended for routine cloning.
Error rate comparable to Pfu and Kod DNA polymerases, but significantly lower than Taq DNA polymerases...
Description:
dNTP Set NB-60-0004 consists of a series of separate Ready-to-use molecular grade dNTP solutions for DNA polymerization.
It contains dATP, dGTP, dCTP, and dTTP at a concentration of 100 mM.
It is supplied in sodium salt solution at pH 8.5 (22 °C).
Ideal for DNA labeling and sequencing applications.
Features:
Ultra-pure: >99% trisphosphate...
Description
The Neo Biotech Gelpure kit (NB-60-0002) purifies DNA fragments from TAE/TBE agarose gels and PCR products (50 bp to 20 kb) with a recovery rate of 60-90% (depending on fragment size).
It uses a silica-gel membrane that selectively adsorbs DNA fragments(<20 μg).
The kit's binding buffer includes a pH indicator for assessing optimal DNA binding pH without affecting the purification process...
Description
Neo Biotech's miniprep kits (NB-60-0001) offer a fast and efficient way to extract pure plasmid DNA from Escherichia coli.
The process includes alkaline lysis of bacterial cells and DNA binding to silica under high salt conditions.
The resulting DNA is ideal for PCR, automated fluorescent sequencing, and various enzymatic applications.
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