Procurou por: SMPB+(N-Succinimidyl+4-(4-Maleimidophenyl)butyrate)

Código de Artigo: (BC21)

Fornecedor: G-Biosciences

Descrição: Succinimidyl 4-(ρ-maleimidophenyl) butyrate Heterobifunctional Cross Linkers.

UOM: 1 * 100 mg

Promoção

Código de Artigo: (TCIAS0861-10MG)

Fornecedor: TCI

Descrição: SMPB (N-Succinimidyl 4-(4-Maleimidophenyl)butyrate) 97,0 HPLC_ASSAY_METHOD

UOM: 1 * 10 mg

Promoção

Código de Artigo: (APOSBICL200-100MG)

Fornecedor: Apollo Scientific

Descrição: Primary amine and Sulphhydryl reactive.Enzyme antibody conjugation - Spacer arm.

UOM: 1 * 100 mg

Promoção

Código de Artigo: (BC24)

Fornecedor: G-Biosciences

Descrição: Sulfo succinimidyl 4-(ρ-maleimidophenyl) butyrate

UOM: 1 * 100 mg

Promoção

Código de Artigo: (APOSBICL201-100MG)

Fornecedor: Apollo Scientific

Descrição: Primary amine and Sulphhydryl reactiveSpacer arm -Water soluble

UOM: 1 * 100 mg

Promoção

Código de Artigo: (PIER22416)

Fornecedor: Thermo Fisher Scientific

Descrição: Thermo Scientific Pierce SMPB is an amine-to-sulfhydryl crosslinker that contains NHS-ester and maleimide reactive groups at opposite ends of a medium-length aromatic spacer arm (11.6 angstroms).

UOM: 1 * 50 mg

Promoção

Código de Artigo: (PIER22317)

Fornecedor: Thermo Fisher Scientific

Descrição: Thermo Scientific Pierce Sulfo-SMPB is a water-soluble amine-to-sulfhydryl crosslinker that contains NHS-ester and maleimide reactive groups at opposite ends of a medium-length aromatic spacer arm (11.6 angstroms).

UOM: 1 * 50 mg

Promoção

Código de Artigo: (PIER22305)

Fornecedor: Thermo Fisher Scientific

Descrição: Thermo Scientific Pierce MPBH is a long, maleimide-and-hydrazide crosslinker for conjugating sulfhydryls (cysteines) to carbonyls (aldehyde or ketones, such as those formed by oxidation of glycoprotein carbohydrates).

UOM: 1 * 50 mg

Promoção

Código de Artigo: (PIER23013)

Fornecedor: Thermo Fisher Scientific

Descrição: Thermo Scientific Pierce SPB is an NHS-ester and psoralen crosslinker that effectively conjugates primary amines to DNA via light-activated intercalation next to pyrimidine bases.

UOM: 1 * 50 mg

Promoção

Código de Artigo: (C1484-25MG)

Fornecedor: SIGMA ALDRICH MICROSCOPY

Descrição: 7-Diethylamino-3-(4-maleimidophenyl)-4-methylcoumarin has been used: as a nontoxic substitute for conjugation with antibody(93) to aid fluorescent detection of Coenzyme A (CoA-SH) in human N-myristoyltransferases assay (94)

UOM: 1 * 25 mg

Promoção

Código de Artigo: (BC18)

Fornecedor: G-Biosciences

Descrição: N-(ρ-Maleimidophenyl) isocyanate Heterobifunctional Cross Linkers.

UOM: 1 * 50 mg

Promoção

Código de Artigo: (APOSBICL223-50MG)

Fornecedor: Apollo Scientific

Descrição: When melted, may contain small amount of sediment Hydroxyl reactive -Thiol reactive

UOM: 1 * 50 mg

Promoção

Código de Artigo: (APOSBII108-100MG)

Fornecedor: Apollo Scientific

Descrição: Sulphhydryl reactive -Iodinatable

UOM: 1 * 100 mg

Promoção

Fornecedor: TCI

Descrição: Bis(3-ethyl-5-methyl-4-maleimidophenyl)methane 98,0 N_ASSAY_METHOD

Fornecedor: TCI

Descrição: 2,2-Bis[4-(4-maleimidophenoxy)phenyl]propane 98,0 HPLC, N

Código de Artigo: (SIAL49667-50MG-F)

Fornecedor: Merck

Descrição: SPB is an amine-reactive and photoreactive heterobifunctional crosslinking reagent. The photoreactive psoralen group provides much greater covalent insertion yields than phenyl azide-containing compounds, which makes this reagent a superior alternative to typical photoreactive NHS-ester crosslinkers. The psoralen tricyclic planar ring system intercalates into double-stranded, and to a lesser extent, single-stranded, DNA, RNA, PCR products, cDNA or oligonucleotides. It also can be used with agarose gel-purified oligonucleotides because the presence of agarose does not interfere with the coupling reaction. The nucleic acid labeling site of the psoralen group (the 5,6 double bond in thymine residues) does not interfere with subsequent hybridization reactions, creating a highly-sensitive direct labeling alternative to radioactive probes.

UOM: 1 * 50 mg

Promoção