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118880 Results for: "9-Cyano-N,N,N\u2032-triethylpyronine-N\u2032-caproic+acid+N-hydroxysuccinimide+ester+chloride"

2-Cyano-4-(trifluoromethyl)benzeneboronic acid neopentyl glycol ester

Supplier: Apollo Scientific

2-Cyano-4-(trifluoromethyl)benzeneboronic acid neopentyl glycol ester

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4-Cyano-3-pyridineboronic acid pinacol ester

Supplier: Apollo Scientific

4-Cyano-3-pyridineboronic acid pinacol ester

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(2Z,4E)-5-Amino-2-cyano-3-methylpenta-2,4-dienoic acid ethyl ester

Supplier: Apollo Scientific

(2Z,4E)-5-Amino-2-cyano-3-methylpenta-2,4-dienoic acid ethyl ester

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3-Cyano-1-propylboronic acid pinacol ester 96%

Supplier: Thermo Fisher Scientific

3-Cyano-1-propylboronic acid pinacol ester 96%

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2-Cyano-3-(3,4-dichloro-phenyl)-acrylic acid ethyl ester

Supplier: Apollo Scientific

2-Cyano-3-(3,4-dichloro-phenyl)-acrylic acid ethyl ester

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4-Cyano-5-methylsulphanylthiophene-2-carboxylic acid methyl ester 97%

Supplier: Thermo Fisher Scientific

4-Cyano-5-methylsulphanylthiophene-2-carboxylic acid methyl ester 97%

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5(6)-Carboxyfluorescein N-hydroxysuccinimide ester (5/6-FAM SE) ≥98% (by TLC)

Supplier: Biotium

5(6)-FAM SE (full name: 5-(and-6)-Carboxyfluorescein, succinimidyl ester mixed isomers) is an amine-reactive green fluorescent dye widely used for labeling proteins or other molecules that contain a primary or secondary aliphatic amine. The coupling reaction is usually carried out at pH 8-9.5. The amide linkage from the coupling reaction is much more stable than the thiourea linkage formed from the coupling of an amine and an isothiocyanate.

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2,5-dioxopyrrolidin-1-yldodecanoate, lyophilised powder

Supplier: MP Biomedicals

Lauric acid N-hydroxysuccinimide ester may be used for the synthesis of N-acylamino acids and lipidisation of polypeptides or other applications that use N-hydroxysuccinimide ester conjugation chemistry.

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D-Biotin-N-succinimidyl ester ≥98%

Supplier: Thermo Fisher Scientific

D-Biotin-N-succinimidyl ester ≥98%

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3-Chloro-5-cyano-2-fluorophenylboronic acid, pinacol ester 96%

Supplier: Apollo Scientific

3-Chloro-5-cyano-2-fluorophenylboronic acid, pinacol ester 96%

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4-Cyano-1H-indole-2-boronic acid, pinacol ester 95%

Supplier: Apollo Scientific

4-Cyano-1H-indole-2-boronic acid, pinacol ester 95%

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2-Cyano-4-(trifluoromethyl)phenylboronic acid pinacol ester

Supplier: Apollo Scientific

2-Cyano-4-(trifluoromethyl)phenylboronic acid pinacol ester

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6-Carboxyfluorescein-N-succinimidyl ester (6-FAM SE) ≥95%

6-Carboxyfluorescein-N-succinimidyl ester (6-FAM SE) ≥95%

Supplier: AAT BIOQUEST

6-FAM, SE is the amine-reactive succinimidyl ester of single isomer 6-FAM acid.

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2-Cyano-3,3-bismethylsulphanylacrylic acid methyl ester 95%

Supplier: Apollo Scientific

2-Cyano-3,3-bismethylsulphanylacrylic acid methyl ester 95%

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D-Biotin-N-succinimidyl ester 98%

D-Biotin-N-succinimidyl ester 98%

Supplier: Thermo Fisher Scientific

D-Biotin-N-succinimidyl ester 98%

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(2E,4E)-2-Cyano-5-phenyl-penta-2,4-dienoic acid methyl ester

Supplier: Apollo Scientific

(2E,4E)-2-Cyano-5-phenyl-penta-2,4-dienoic acid methyl ester

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Sulpho-NHS (N-Hydroxysulphosuccinimide sodium salt)

Supplier: G-Biosciences

Sulpho-NHS reacts primarily with primary amines to convert carboxyl groups to amine reactive sulfo-NHS esters. It is ideal for cross-linking, chemical labelling and solid support immobilisation. It is used to generate amine reactive esters from carboxylate groups and is primarily used to increase the efficiency of the carbodiimide EDC cross-linking. EDC reactions do not require Sulpho-NHS; however, its presence greatly enhances cross-linking efficiency and allows for a two-step process. EDC reacts with a carboxylate group to form an active ester, which is subject to rapid hydrolysis in aqueous buffers. The Sulfo-NHS increases the stability of the active intermediate and the resulting coupled product is identical to EDC reactions without sulpho-NHS.

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Caproic acid 99%

Supplier: Apollo Scientific

Caproic acid 99%

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Caproic acid 99%

Caproic acid 99%

Supplier: Thermo Fisher Scientific

Caproic acid 99%

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4-(2-Cyano-3-ethoxy-3-oxo-1-propen-1-yl)benzeneboronic acid pinacol ester 97%

Supplier: Thermo Fisher Scientific

4-(2-Cyano-3-ethoxy-3-oxo-1-propen-1-yl)benzeneboronic acid pinacol ester 97%

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Acridinium C2 NHS Ester for biomolecular labeling

Acridinium C2 NHS Ester for biomolecular labeling

Supplier: AAT BIOQUEST

The acridinium NHS ester can be used to label proteins and nucleic acids.

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N-Succinimidyl 3-Maleimidobenzoate 95%

Supplier: Thermo Fisher Scientific

MBS (N-Succinimidyl 3-maleimidobenzoate) 95%

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Ethyl (R)-(-)-4-cyano-3-hydroxybutyate 98%

Supplier: Thermo Fisher Scientific

Ethyl (R)-(-)-4-cyano-3-hydroxybutyate 98%

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Methyl 5-cyano-2-fluorobenzoate 95%

Supplier: Apollo Scientific

Methyl 5-cyano-2-fluorobenzoate 95%

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Ethyl-2-cyano-2-methylpropionate 98%

Supplier: Apollo Scientific

Ethyl-2-cyano-2-methylpropionate 98%

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2-Ethylhexyl-2-cyano-3,3-diphenylacrylate

Supplier: Apollo Scientific

2-Ethylhexyl-2-cyano-3,3-diphenylacrylate

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Ethyl-2-cyano-2-methylpropionate 97%

Supplier: Thermo Fisher Scientific

Ethyl-2-cyano-2-methylpropionate 97%

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MBS (N-Succinimidyl 3-maleimidobenzoate), Pierce™

MBS (N-Succinimidyl 3-maleimidobenzoate), Pierce™

Supplier: Thermo Fisher Scientific

Thermo Scientific Pierce MBS is an amine-to-sulfhydryl crosslinker that contains NHS-ester and maleimide reactive groups at opposite ends of a short aromatic spacer arm (7.3 angstroms).

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Ethyl cyano(hydroxyimino)acetate

Supplier: Apollo Scientific

Ethyl cyano(hydroxyimino)acetate

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6-Carboxyfluorescein-N-succinimidyl ester (6-FAM SE) ≥99% (by TLC) amine-reactive fluorescent dye

Supplier: Biotium

6-FAM, SE (full name: 6-Carboxyfluorescein, succinimidyl ester, single isomer) is the amine-reactive form of 6-carboxyfluorescein single isomer.
6-FAM SE is an amine-reactive green fluorescent dye widely used for labeling oligonucleotides or other biomolecules that contain a primary or secondary aliphatic amine. The coupling reaction is usually carried out at pH 8-9.5.

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