Reagents, S

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  • Features   Synonym: Soda Ash CAS#: 497-19-8 Molecular Formula: Na2CO3 Molecular Weight: 105.99

  • Sodium L-Lactate

    G-Biosciences

    L-lactate is produced from pyruvate by the enzyme Lacate Dehydrogenase. Lactate production occurs during anaerobic glycolysis or in proliferatively active cells. Store at 2-8°C Features Synonyms: L-Lactic Acid Sodium Salt, (S)-2-Hydroxypropionic acid sodium salt, Sarcolactic…

  • HOOK™ Sulfo-NHS-LC-LC-Biotin reacts with protein primary amines.Amines, lysine ε-amines and N-terminal α-amines, are the most abundant group in protein molecules and represent the most common target for biotinylation. For example, BSA contains 59 primary amines, of which up to…

  • Sodium Hydroxide

    G-Biosciences

    Features CAS#: 1310-73-2 Molecular Formula: NaOH Molecular Weight: 40.00

  • Convenient solution of 1% sodium azide minimizes exposure and contamination risks normally encountered while handling sodium azide powder. Features CAS #: 26628-22-8 Molecular Formula: NaN3 Molecular Weight: 65.0099

  • Sulfosuccinimidyl-2-(ρ-azidosalicylamido)ethyl-1,3-dithiopropionate Features Molecular Weight: 541.51 Spacer Arm (Å): 18.9 Reactive Toward: Primary Amines Membrane Permeable: NO Water Soluble: YES Cleavable/ Reversible: Reducing Agents (Thiol)

  • HOOK™-sulfo-NHS-Biotin

    G-Biosciences

    HOOK™ Sulfo-NHS-Biotin reacts with protein primary amines. Amines, lysine ε-amines and N-terminal α-amines, are the most abundant group in protein molecules and represent the most common target for biotinylation. For example, BSA contains 59 primary amines, of which up to 35 are…

  • Sulfodisuccinimidyl tartrate Features Molecular Weight: 548.32 Spacer Arm (Å): 6.4 Reactive Toward: Primary Amines Membrane Permeable: NO Water Soluble: YES Cleavable/ Reversible: Oxidizing Agents (Periodate)

  • Features Chemical Name: N- Hydroxysulfosuccinimide Reacts primarily with primary amines Water soluble Molecular weight: 217.13 Applications Ideal for cross-linking, chemical labeling and solid support immobilization Increase efficiency of EDC coupling Convert…

  • Sodium Cyanoborohydride

    G-Biosciences

    Carbonyl groups, including aldehydes, ketones and glyoxals, react with amines to form Schiff base intermediates that are in equilibrium with their free forms.The labile Schiff’s base interaction can be stabilized by chemical reduction. If the Schiff’s base is formed between an aldehyde…

  • Sulfosuccinimidyl 2-( m -azido- o -nitrobenzamido)-ethyl-1,3’-dithiopropionate Features Molecular Weight: 570.51 Spacer Arm (Å): 18.5 Reactive Toward: Primary Amines Membrane Permeable: NO Water Soluble: YES Cleavable/ Reversible: Reducing Agents (Thiol)

  • HOOK™ Sulfo-NHS-SS-Biotin reacts with protein primary amines.Amines, lysine ε-amines and N-terminal α-amines, are the most abundant group in protein molecules and represent the most common target for biotinylation. For example, BSA contains 59 primary amines, of which up to 35…

  • N -(ε-Maleimidocaproyloxy) sulfo succinimide ester Features Molecular Weight: 410.33 Spacer Arm (Å): 9.4 Reactive Toward: Primary Amine + Sulfhydryl Membrane Permeable: NO Water Soluble: YES Cleavable/ Reversible: NO

  • N -Hydroxysulfosuccinimidyl-4-azidobenzoate Features Molecular Weight: 362.25 Spacer Arm (Å): 9.0 Reactive Toward: Primary Amines Membrane Permeable: NO Water Soluble: YES Cleavable/ Reversible: NO

  • Features Synonym: Acetic acid sodium salt CAS#: 127-9-3 Molecular Formula: C2H3O2Na Molecule Weight: 82.03

  • Sodium metaperiodate

    G-Biosciences

    Sodium metaperiodate, or sodium m-periodate, is a mild oxidant that is routinely used for the conversion of cis -glycol groups in carbohydrates to reactive aldehdye groups (Figure 1).The reactive aldehyde groups are used in chemical conjugation procedures or detection of carbohydrates.For…

  • Sulfosuccinimidyl 4-( N -maleimidomethyl) cyclohexane-1-carboxylate Ideal for enzyme-antibody crosslinking OneQuant ™ Sulfo SMCC is also available: Single use vials to minimize waste. No weighing required. Features Synonym: Water Soluble SMCC CAS Number: …

  • Sulfo succinimidyl 4-(ρ-maleimidophenyl) butyrate Features Molecular Weight: 458.38 Spacer Arm (Å): 14.5 Reactive Toward: Primary Amine + Sulfhydryl Membrane Permeable: NO Water Soluble: YES Cleavable/ Reversible: NO

  • HOOK™-Sulfo-NHS-LC-Biotin reacts with protein primary amines.Amines, lysine ε-amines and N-terminal α-amines, are the most abundant group in protein molecules and represent the most common target for biotinylation. For example, BSA contains 59 primary amines, of which up to 35…

  • Succinimidyl 4-(ρ-maleimidophenyl) butyrate Ideal for enzyme-antibody crosslinking Features Molecular Weight: 356.33 Spacer Arm (Å): 11.6 Reactive Toward: Primary Amine + Sulhydryl Membrane Permeable: YES Water Soluble: NO Cleavable/ Reversible: NO

  • N -Succinimidyl(4-iodoacetyl)aminobenzoate Ideal for enzyme-antibody crosslinking Features Molecular Weight: 402.14 Spacer Arm (Å): 10.6 Reactive Toward: Primary Amine + Sulfhydryl Membrane Permeable: YES Water Soluble: NO Cleavable/ Reversible: NO

  • N -γ-Maleimidobutyryloxysulfosuccinimide ester Features Molecular Weight: 382.38 Spacer Arm (Å): 6.8 Reactive Toward: Primary Amine + Sulfhydryl Membrane Permeable: NO Water Soluble: YES Cleavable/ Reversible: NO

  • N -Sulfosuccinimidyl(4-iodoacetyl)aminobenzoate Features Molecular Weight: 504.19 Spacer Arm (Å): 10.6 Reactive Toward: Primary Amine + Sulfhydryl Membrane Permeable: NO Water Soluble: YES Cleavable/ Reversible: NO

  • m -Maleimidobenzoyl- N -hydroxysulfosuccinimide ester Features Molecular Weight: 416.30 Spacer Arm (Å): 9.9 Reactive Toward: Primary Amine + Sulfhydryl Membrane Permeable: NO Water Soluble: YES Cleavable/ Reversible: NO

  • Sodium Oxamate

    G-Biosciences

    Sodium Oxamate is a known glycolysis inhibitor. It inhibits the conversion of pyruvate to lactate via lactate dehydrogenase (LDH). Sodium oxamate has been studied as an inhibitor of carbohydrate metabolism in various tumors, as cancer cells are often dependent on glycolysis for ATP production. …

  • Succinimidyl 4-( N -maleimidomethyl) cyclohexane-1-carboxylate Ideal for enzyme-antibody crosslinking Features Molecular Weight: 334.32 Spacer Arm (Å): 11.6 Reactive Toward: Primary Amine + Sulfhydryl Membrane Permeable: YES Water Soluble: NO …

  • Features Chemical Name: N-Succinimidyl S-acetylthioacetate CAS Number: 76931-93-6 Molecular Weight: 245.25 Reacts primarily with primary amines Adds protected sulfhydryl residues Sulfhydryl group can be used in coupling reactions Soluble in DMSO Chemical…

  • Sulfo SHPP

    G-Biosciences

    G-Biosciences water-soluble Bolton-Hunter Reagent (Sulfo-SHPP) conjugates tyrosine-like groups to end-terminal α-amino groups or ε-amino groups of lysineto increase the number of tyrosyl groups that can be iodinated by iodine-125 labeling procedures. Radioactive iodine ( 125 I)…

  • Sulfo-SANPAH N-Sulfosuccinimidyl-6-(4'-azido-2'-nitrophenylamino) hexanoate Photoreactive Crosslinker Sulfo-SANPAH is a water-soluble crosslinker with a long spacer-arm (18.2 angstrom) that contains an amine-reactive N-hydroxysuccinimide (NHS) ester and a photoactivatable…

  • Sulfosuccinimidyl (4-azidophenyl)-1,3’-dithiopropionate Features Molecular Weight: 454.44 Spacer Arm (Å): 13.9 Reactive Toward: Primary Amines Membrane Permeable: NO Water Soluble: YES Cleavable/ Reversible: Reducing Agents (Thiol)

  • Features Chemical Name: Sulfosuccinimidyl acetate Reacts primarily with primary amines Reacts at pH 7-9 Water soluble Molecular weight: 259.17 Applications Blocks primary amines by acylation

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