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%
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%
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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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
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™
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.