High quality proteomic grade β-mercaptoethanol. β-mercaptoethanol, a popular reducing agent, is offered in 5ml and 100ml bottles. Features Synonym: β-Mercaptoethanol CAS#: 60-24-2 Molecular Formula: C₂H₆OS Molecular Weight: 78.13 …

( Bis (2-[Succinimidooxycarbonyloxy]ethyl) sulfone Features Molecular Weight: 436.35 Spacer Arm (Å): 13 Reactive Toward: Primary Amines Membrane Permeable: YES Water Soluble: NO Cleavable/ Reversible: Base

HOOK™ NHS-Biotin reacts with protein primary amines. Amines, lysine ε-amines and N-terminal α-amines, are the most abundant group in protein molecules and represent the most common target for biotinylation. For example, BSA contains 59 primary amines, of which up to 35 are…

HOOK™ PFP-Biotin reacts with protein primary amines.Amines, lysine ε-amines and N-terminal α-amines, are the most abundant group in protein molecules and represent the most common target for biotinylation. For example, BSA contains 59 primary amines, of which up to 35 are…

The use of biotin for non-radioactive labeling of proteins and nucleic acids has now become an increasingly popular technique in life science research. Several factors must be considered when coupling a biotin reagent to a protein to ensure a successful reaction. The primary consideration is the…

G-Biosciences Bolton-Hunter Reagent conjugatestyrosine-like groups to end-terminal α-amino groups or ε-amino groups of lysineto increase the number of tyrosyl groups that can be iodinated by iodine-125 labeling procedures. Radioactive iodine ( 125 I) is routinely used by…

HOOK™ Biotin-BMMCC reacts with protein free sulhydryl groups. Sulfhydryl reactive reagents are more specific and react only with free sulfhydryl residues (-SH or thiol groups). The side chain of the amino acid cysteine is the most common source of free sulfhydryl groups. If free sulfhydryl…

Features Molecular Weight: 244.32

HOOK™ NHS-LC-LC-Biotin reacts with protein primary amines.Amines, lysine ε-amines and N-terminal α-amines, are the most abundant group in protein molecules and represent the most common target for biotinylation. For example, BSA contains 59 primary amines, of which up to 35 are…

The use of biotin for non-radioactive labeling of proteins and nucleic acids has become an increasingly popular technique in life science research. Several factors must be considered when coupling a biotin reagent to a protein in order to ensure a successful reaction. The primary consideration is…

The use of biotin for non-radioactive labeling of proteins and nucleic acids has now become an increasingly popular technique in life science research. Several factors must be considered when coupling a biotin reagent to a protein to ensure a successful reaction. The primary consideration is the…

HOOK™ NHS-SS-Biotin reacts with protein primary amines.Amines, lysine ε-amines and N-terminal α-amines, are the most abundant group in protein molecules and represent the most common target for biotinylation. For example, BSA contains 59 primary amines, of which up to 35 are…

HOOK™ Iodoacetyl-LC-Biotin reacts with protein free sulhydryl groups. Sulfhydryl reactive reagents are more specific and react only with free sulfhydryl residues (-SH or thiol groups). The side chain of the amino acid cysteine is the most common source of free sulfhydryl groups. If free…

Blue-OUT™ is a unique product that washes the interfering Coomassie and fluorescent protein stains from gel pieces prior to their treatment for protein sequencing or mass spectrometry. Also supplied in the InGel™ Blue kit for the tryptic digestion and peptide extraction of…

HOOK™ NHS-dPEG™4-Biotin reacts with protein primary amines.Amines, lysine ε-amines and N-terminal α-amines, are the most abundant group in protein molecules and represent the most common target for biotinylation. For example, BSA contains 59 primary amines, of which up to…

The use of biotin for non-radioactive labeling of proteins and nucleic acids has now become an increasingly popular technique in life science research. Several factors must be considered when coupling a biotin reagent to a protein to ensure a successful reaction. The primary consideration is the…

HOOK™-NHS-LC-Biotin reacts with protein primary amines. Amines, lysine ε-amines and N-terminal α-amines, are the most abundant group in protein molecules and represent the most common target for biotinylation. For example, BSA contains 59 primary amines, of which up to 35 are…

The use of biotin for non-radioactive labeling of proteins and nucleic acids has become an increasingly popular technique in life science research. Several factors must be considered when coupling a biotin reagent to a protein in order to ensure a successful reaction. The primary consideration is…

HOOK™ PEG₂-Iodoacetyl-Biotin reacts with protein free sulhydryl groups. Sulfhydryl reactive reagents are more specific and react only with free sulfhydryl residues (-SH or thiol groups). The side chain of the amino acid cysteine is the most common source of free sulfhydryl…

Bis (β-[4-azidosalicylamido]-ethyl) disulfide Iodinatable Features Molecular Weight: 474.52 Spacer Arm (Å): 21.3 Reactive Toward: Non Selective Membrane Permeable: YES Water Soluble: NO Cleavable/ Reversible: Reducing Agents (Thiols)

HOOK™ Biotin-PDA reacts with protein free sulhydryl groups. Sulfhydryl reactive reagents are more specific and react only with free sulfhydryl residues (-SH or thiol groups). The side chain of the amino acid cysteine is the most common source of free sulfhydryl groups. If free sulfhydryl…