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Catalog Number: (BC17)
Supplier: G-Biosciences
Description: N-(ε-Maleimidocaproyloxy) sulfo succinimide ester Heterobifunctional Cross Linker.
UOM: 1 * 50 mg


Supplier: SIGMA ALDRICH MICROSCOPY
Description: 4-(N-Maleimidomethyl)cyclohexane-1-carboxylic acid 3-sulfo-N-hydroxysuccinimide ester sodium salt,powder (Sulfo-SMCC)

Catalog Number: (BC14)
Supplier: G-Biosciences
Description: N-γ-Maleimidobutyryloxysulfosuccinimide ester Heterobifunctional Cross Linker.
UOM: 1 * 100 mg


Supplier: Thermo Fisher Scientific
Description: Thermo Scientific EZ-Link Sulfo-NHS-LC-LC-Biotin enables simple and efficient biotin labeling of antibodies, proteins, and any other primary amine–containing macromolecules. Specific labeling of cell surface proteins is another common application for these uniquely water-soluble and membrane impermeable reagents.

Catalog Number: (BC12)
Supplier: G-Biosciences
Description: m-Maleimidobenzoyl-N-hydroxysulfosuccinimide esterHeterobifunctional Cross Linker
UOM: 1 * 100 mg


Catalog Number: (APOSBICL203-100MG)
Supplier: Apollo Scientific
Description: Primary amine and sulphhydryl reactive -Water soluble
UOM: 1 * 100 mg


Catalog Number: (APOSBICL101-100MG)
Supplier: Apollo Scientific
Description: Primary amine reactive -Membrane impermeableWater soluble.
UOM: 1 * 100 mg


Catalog Number: (BC23)
Supplier: G-Biosciences
Description: Ideal for enzyme-antibody crosslinking.
UOM: 1 * 100 mg


Supplier: Thermo Fisher Scientific
Description: Thermo Scientific Pierce Premium Grade Sulfo-NHS is our highest quality formulation of this N-hydroxysuccinimide chemical modification reagent, specially characterized for applications where product integrity and risk minimization are paramount.

Catalog Number: (PIER26777)
Supplier: Thermo Fisher Scientific
Description: Pierce™ Sulfo-NHS-Acetate is a small compound used for blocking primary amines (eg. lysine side chains). This compound forms stable, covalent amide bonds with amine groups to prevent specific interactions or conjugations.
UOM: 1 * 100 mg


Catalog Number: (BC07)
Supplier: G-Biosciences
Description: Dithiobis(succinimidyl propionate) Homobifunctional Cross Linker.
UOM: 1 * 1 g


Supplier: Thermo Fisher Scientific
Description: Sulpho-SMCC (3-Sulpho-N-succinimidyl-4-(N-maleimidomethyl)cyclohexane-1-carboxylate sodium salt) ≥97%
Catalog Number: (APOSBICL207-100MG)
Supplier: Apollo Scientific
Description: Primary amine & Sulphhydryl reactiveEnzyme-antibody conjugation -Stable maleimide groupRef: Hushida, S. et al (1984) J.Applied Biochem. 56,56-63
UOM: 1 * 100 mg


Catalog Number: (SIAL803340-50MG)
Supplier: Merck
Description: Succinimidyl-diazirine (SDA) reagents are a new class of crosslinkers that combine proven amine-reactive chemistry with an innovative and efficient diazirine-based photochemistry for conjugating amine-containing molecules to nearly any other functional group. The SDA crosslinkers include six compounds differing in spacer arm lengths, ability to cleave the crosslinked proteins, and presence or absence of a charged group for membrane permeability. Protein crosslinking is an important technique used to understand protein structure and to stabilize protein-protein interactions, and these SDA reagents extend the efficiency and range of interactions that can be explored by this approach.
UOM: 1 * 50 mg


Catalog Number: (APOSBIPG1317-50MG)
Supplier: Apollo Scientific
Description: Bromoacetamido-PEG4- NHS ester
UOM: 1 * 50 mg


Catalog Number: (SIAL803359-50MG)
Supplier: Merck
Description: Succinimidyl-diazirine (SDA) reagents are a new class of crosslinkers that combine proven amine-reactive chemistry with an innovative and efficient diazirine-based photochemistry for conjugating amine-containing molecules to nearly any other functional group. The SDA crosslinkers include six compounds differing in spacer arm lengths, ability to cleave the crosslinked proteins, and presence or absence of a charged group for membrane permeability. Protein crosslinking is an important technique used to understand protein structure and to stabilize protein-protein interactions, and these SDA reagents extend the efficiency and range of interactions that can be explored by this approach.
UOM: 1 * 50 mg


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