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19450 Results for: "Bromoacetamido-PEG4-+NHS+ester&amp"

Bromoacetamido-PEG4- NHS ester

Supplier: Apollo Scientific

Bromoacetamido-PEG4- NHS ester

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SBAP (Succinimidyl 3-(bromoacetamido)propionate)

Supplier: Apollo Scientific

SBAP (Succinimidyl 3-(bromoacetamido)propionate)

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Mal-amido-PEG4-NHS

Supplier: Apollo Scientific

Mal-amido-PEG4-NHS

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SBAP (Succinimidyl 3-(bromoacetamido)propionate), Pierce™

SBAP (Succinimidyl 3-(bromoacetamido)propionate), Pierce™

Supplier: Thermo Fisher Scientific

Thermo Scientific Pierce SBAP is a short (6.2 angstrom) crosslinker for amine-to-sulfhydryl conjugation via N-hydroxysuccinimide (NHS) ester and bromoacetyl reactive groups.

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SBAP (Succinimidyl 3-(bromoacetamido)propionate) ≥90%, Sigma-Aldrich®

Supplier: Merck

SBAP is a sulfhydryl-reactive and amine-reactive heterobifunctional crosslinker. The reagent′s NHS ester reacts with primary amines at pH 7-9 to form stable amide bonds, and the bromacetyl reacts with sulfhydryl groups at pH >7.5 to form stable thioether bonds This reagent is useful for preparing cyclic peptides and peptide conjugates because the spacer maintains peptide-like character in the crosslinked species.

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Azadibenzocyclooctyne-PEG4-NHS ester

Supplier: Thermo Fisher Scientific

Azadibenzocyclooctyne-PEG4-NHS ester (ADIBO-PEG4-NHS ester) is applied for protein-peptide conjugation, peptide-small molecule conjugation, 18F radiolabeling, protein-oligonucleotide conjugation and surface modification.

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Biotin-PEG4-NHS biodetection

Biotin-PEG4-NHS biodetection

Supplier: AAT BIOQUEST

Biotin PEG4 succinimidyl ester is an amine-reactive biotin derivative that contains a long arm to increase its avidin-binding affinity.

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DBCO-PEG4-NHS Ester for biomolecular labeling

DBCO-PEG4-NHS Ester for biomolecular labeling

Supplier: AAT BIOQUEST

Cu-free click reaction, i.e., the strain-promoted alkyne-azide cycloaddition (SPAAC) is a bioorthogonal reaction utilizing a pair of reagents, cyclooctynes and azides that exclusively and efficiently react with each other while remain inert to naturally occurring functional groups such as hydroxy, amino and thiol groups.

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DNP-PEG4-NHS ester FRET quencher precursor

DNP-PEG4-NHS ester FRET quencher precursor

Supplier: AAT BIOQUEST

Compared to the commonly used DNP-X SE (#2021), DNP-PEG4 NHS ester has much better water solubility.

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Fmoc-NH-PEG4-CH2CO2H

Supplier: Apollo Scientific

Fmoc-NH-PEG4-CH2CO2H

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PEGylated SPDP Crosslinkers, Heterobifunctional, Pierce™

PEGylated SPDP Crosslinkers, Heterobifunctional, Pierce™

Supplier: Thermo Fisher Scientific

Cross linkers are used for the identification of near-neighbour protein relationships and ligand-receptor interactions. Homobifunctional, amine-reactive NHS esters or imidates, and heterobifunctional, amine-reactive, photoactivatable phenyl azides are the most commonly used crosslinkers for these applications.

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t-Boc-N-Amido-PEG4-Amine

Supplier: Apollo Scientific

t-Boc-N-Amido-PEG4-Amine

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t-Boc-N-amido-PEG4-alcohol

Supplier: Apollo Scientific

t-Boc-N-amido-PEG4-alcohol

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AMP (2-Amino-2-methylpropanol) for synthesis, Sigma-Aldrich®

Supplier: Merck

AMP (2-Amino-2-methylpropanol) for synthesis, Sigma-Aldrich®

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AMP (2-Amino-2-methylpropanol), high purity

AMP (2-Amino-2-methylpropanol), high purity

Supplier: VWR Chemicals

5% water has been added to maintain liquidity at room temperature.

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Azido-PEG4-PFP ester

Supplier: Apollo Scientific

Azido-PEG4-PFP ester

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Biotin-PEG4-PFP ester

Supplier: Apollo Scientific

Biotin-PEG4-PFP ester

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AMP (2-Amino-2-methylpropanol) 99%

AMP (2-Amino-2-methylpropanol) 99%

Supplier: Thermo Fisher Scientific

AMP (2-Amino-2-methylpropanol) 99%

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Ald-PEG4-t-butyl ester

Supplier: Apollo Scientific

Ald-PEG4-t-butyl ester

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AMP (2-Amino-2-methylpropanol), (max. 5% H₂O) 95%

Supplier: Thermo Fisher Scientific

AMP (2-Amino-2-methylpropanol), (max. 5% H₂O) 95%

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AMP (2-Amino-2-methylpropanol) 95%

Supplier: Apollo Scientific

Used for the preparation of buffer solutions, suitable for the determination of alkaline phosphatase.

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AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

Supplier: Merck

AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

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AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

Supplier: Merck

AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

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AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

Supplier: Merck

AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

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AMP (2-Amino-2-methylpropanol)

Supplier: Molekula

AMP (2-Amino-2-methylpropanol)

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AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

Supplier: Merck

AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

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AMP (2-Amino-2-methylpropanol)

Supplier: Spectrum Chemical

2-Amino-2-methyl-1-propanol, or aminomethyl propanol is a colourless, viscous liquid that functions as a pH adjuster. It is also used as an intermediate in drug synthetic schemes.

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Anti-HINT1 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Supplier: Bioss

The protein encoded by this gene can hydrolyse substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumour suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene.

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Anti-HINT1 Rabbit Polyclonal Antibody

Supplier: Bioss

The protein encoded by this gene can hydrolyze substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumor suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012].

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Anti-HINT1 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Supplier: Bioss

The protein encoded by this gene can hydrolyze substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumor suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012].

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