Protein Labeling Reagents
Sigma Aldrich Fine Chemicals Biosciences Sera MagTM Magnetic carbox
Sera-Mag(TM) SpeedBeads(TM) and Sera-Mag(TM) Carboxylate-Modified Magnetic Particles combine a fast magnetic response time and high binding capacity with a large surface area high sensitivity stability physical integrity and fast reaction kinetics. Covalent coupling of biomolecules such as proteins and nucleic acids to carboxyl groups on the surface is easily accomplished using our standard coupling technology. The core of the particle is made by a free radical emulsion polymerization of styrene and acid monomer. One (Sera-Mag(TM)) or two (Sera-Mag(TM) SpeedBeads(TM)) layers of magnetite are then coated onto this core while the surface is modified to minimize non-specific binding of proteins.
Lumiprobe Sulfo-Cyanine7 NHS ester | 1603861-95-5 | MFCD28385520 | 1 mg
Sulfo-Cyanine7 NHS ester | Purity: 95% | Mol Wt: 844.05 | 1603861-95-5 | MFCD28385520 | 1 mg
Bachem 5-Carboxy-fluorescein
5-Carboxy-fluorescein, 76823-03-5, C21H12O7, Mr 376.32, 500mg. 5-FAM, 4-(6-Hydroxy-3-oxo-3H-xanthen-9-yl)-isophthalic acid. Widely used green-fluorescent labeling dye.
MilliporeSigma IHC Select HRP/DAB, 150 Test
IHC Select HRP/DAB Tests for Immunocytochemistry, Immunohistochemistry & Immunohistochemistry (Paraffin). The IHC Select Immunoperoxidase Secondary Detection System is intended for use with the CHEMICON IHC Select Prediluted Primary Antibody reagents which contain rabbit and mouse IgG for the qualitative identification of antigens by light microscopy in paraffin-embedded tissues. The IHC Select Immunoperoxidase Secondary Detection System may also be used with other rabbit or mouse IgG primary antibodies.
Jackson Immuno Research Labs Rhodamine Red™-X (RRX) AffiniPure Donkey Anti-Goat IgG (H+L), .5mg
Rhodamine Red-X-AffiniPure Donkey Anti-Goat IgG (H+L) (min X Ck,GP,Sy Hms,Hrs,Hu,Ms,Rb,Rat Sr Prot)
Aat Bioquest SDA azide, 1mg
SDA azide contains both diazirine photoaffinity moiety and azide functional group. It is an excellent building block to introduce photoaffinity function into an alkyne-modified biomolecule via the well-known click chemistry. Diazirines are known for their ability to undergo photochemical reactions when exposed to ultraviolet (UV) light, specifically by forming highly reactive carbene intermediates that react with nearby molecules, forming covalent bonds. This property makes diazirines useful for studying protein-protein, protein-nucleic acid interactions, ligand-receptor binding, and other biomolecular interactions. It's important to note that diazirines are highly reactive and can be challenging to handle due to their instability. They require careful storage and handling, typically in a controlled environment.