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17705 results for "Isonicotinamidine+hydrochloride"

17705 Results for: "Isonicotinamidine+hydrochloride"

Urea, white prills, Reagent Grade

Supplier: MP Biomedicals

Urea is a prinicipal protein metabolite end product of nitrogen metabolism in most mammals, formed by the enzymatic reactions of the Kreb's cycle and the major product for the removal of free ammonia (NH4+) in vivo.

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Compatible Lowry protein assay

Supplier: G-Biosciences

These CL (Compatible Lowry) Protein Assay is based on the widely cited protein assay by Lowry et. al. (1951). The CL Protein Assay improves upon the traditional Lowry method to be compatible with common laboratory agents known to interfere with Lowry protein assays such as reducing agents (dithiothreitol (DTT), ß-mercaptoethanol and TCEP), detergents, chelating agents, amines, sugars, strong chaotropic buffers, salts, drugs, antibiotics, cobalt and other common laboratory agents.

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Affinity coupling media, Epoxy-Activated Sepharose™ 6B

Supplier: Cytiva

Epoxy-activated Sepharose™ 6B is a pre-activated medium for immobilisation of various ligands including sugars through coupling of hydroxy, amino or thiol groups on the ligand to Sepharose™ 6B via a 12-atom hydrophilic spacer arm. Medium is formed by reacting Sepharose™ 6B with 1,4-bis (2,3- epoxy-propoxy-) butane. It can be used to couple sugars and other carbohydrates via stable ether linkages to hydroxyl groups.

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Urea ≥99%, white prills, Ultrapure

Supplier: MP Biomedicals

Urea is the principal end product of nitrogen metabolism in most mammals, formed by the enzymatic reactions of the Kreb's cycle.

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Ion exchange chromatography media, IEX Sepharose™ Fast Flow

Ion exchange chromatography media, IEX Sepharose™ Fast Flow

Supplier: Cytiva

Q Sepharose Fast Flow is part of the Sepharose Fast Flow ion exchange platform, which has been the industrial standard for ion exchange chromatography during recent decades.

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Affinity chromatography media, Heparin Sepharose™ 6 Fast Flow

Affinity chromatography media, Heparin Sepharose™ 6 Fast Flow

Supplier: Cytiva

Heparin Sepharose 6 Fast Flow is composed of cross-linked 6% agarose beads modified sodium heparin. Immobilization is performed using chemically stable and oriented coupling giving high binding capacity. The chemical stability of the media is solely dictated by the heparin ligand. Heparin Sepharose 6 Fast Flow is a member of the Cytiva range of affinity chromatography media for capture and intermediate purification.

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L(+)-Lysine monohydrate, powder

Supplier: MP Biomedicals

L-Lysine is an essential proteinogenic α amino acid. It contains an N-butyl amino group in the side chain, and this moiety is protonated at physiological pH. In addition, L-lysine is one of the two amino acids that are degraded to give ketone bodies (a ketogenic amino acid).

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Anti-bacterial Agent 1 * 25 g

Supplier: MP Biomedicals

Anti-bacterial Agent 1 * 25 g

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Anti-bacterial Agent 1 * 50 g

Supplier: MP Biomedicals

Anti-bacterial Agent 1 * 50 g

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Purity: 98% 1 * 1 g

Supplier: MP Biomedicals

Purity: 98% 1 * 1 g

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Tetracycline is a bacteriostatic antibiotic with activity against both gram-positive and gram-negative bacteria. Within the cell tet racycline binds reversibly to the 30S subunit of the ribosome, preventing the binding of aminoacyl tRNA and inhibitin 1 * 25 g

Supplier: G-Biosciences

Tetracycline is a bacteriostatic antibiotic with activity against both gram-positive and gram-negative bacteria. Within the cell tet racycline binds reversibly to the 30S subunit of the ribosome, preventing the binding of aminoacyl tRNA and inhibitin 1 * 25 g

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Atipamezole is an imidazole that potently antagonizes the 2-adrenoceptor (Ki = 1.6 nM).{25705,25706} It shows selectivity over the 1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels.{25706} Th 1 * 5 mg

Supplier: Cayman Chemical

Atipamezole is an imidazole that potently antagonizes the 2-adrenoceptor (Ki = 1.6 nM).{25705,25706} It shows selectivity over the 1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels.{25706} Th 1 * 5 mg

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Rauwolscine is a natural alkaloid that acts as a selective and reversible 2-adregenergic receptor antagonist (Ki = 12 nM).{25653} I t is a stereoisomer of yohimbine, which potently antagonizes both 1- and 2-adrenergic receptors.{25653} Rauwolscine 1 * 250 mg

Supplier: Cayman Chemical

Rauwolscine is a natural alkaloid that acts as a selective and reversible 2-adregenergic receptor antagonist (Ki = 12 nM).{25653} I t is a stereoisomer of yohimbine, which potently antagonizes both 1- and 2-adrenergic receptors.{25653} Rauwolscine 1 * 250 mg

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Purity: 98% 1 * 5 g

Supplier: MP Biomedicals

Purity: 98% 1 * 5 g

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(2S,3S)-3-Hydroxy-2-(4- methoxyphenyl)-2,3-dihydro-1,5- benzothiazepin-4(5H)-one 1 * 25 mg

Supplier: LGC Standards PROMOCHEM

(2S,3S)-3-Hydroxy-2-(4- methoxyphenyl)-2,3-dihydro-1,5- benzothiazepin-4(5H)-one 1 * 25 mg

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Rauwolscine is a natural alkaloid that acts as a selective and reversible 2-adregenergic receptor antagonist (Ki = 12 nM).{25653} I t is a stereoisomer of yohimbine, which potently antagonizes both 1- and 2-adrenergic receptors.{25653} Rauwolscine 1 * 50 mg

Supplier: Cayman Chemical

Rauwolscine is a natural alkaloid that acts as a selective and reversible 2-adregenergic receptor antagonist (Ki = 12 nM).{25653} I t is a stereoisomer of yohimbine, which potently antagonizes both 1- and 2-adrenergic receptors.{25653} Rauwolscine 1 * 50 mg

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Atipamezole is an imidazole that potently antagonizes the 2-adrenoceptor (Ki = 1.6 nM).{25705,25706} It shows selectivity over the 1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels.{25706} Th 1 * 25 mg

Supplier: Cayman Chemical

Atipamezole is an imidazole that potently antagonizes the 2-adrenoceptor (Ki = 1.6 nM).{25705,25706} It shows selectivity over the 1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels.{25706} Th 1 * 25 mg

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Atipamezole is an imidazole that potently antagonizes the 2-adrenoceptor (Ki = 1.6 nM).{25705,25706} It shows selectivity over the 1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels.{25706} Th 1 * 10 mg

Supplier: Cayman Chemical

Atipamezole is an imidazole that potently antagonizes the 2-adrenoceptor (Ki = 1.6 nM).{25705,25706} It shows selectivity over the 1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels.{25706} Th 1 * 10 mg

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Anti-bacterial Agent 1 * 5 g

Supplier: MP Biomedicals

Anti-bacterial Agent 1 * 5 g

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(2S,3S)-5-[2-(Dimethylamino)ethyl]-3- hydroxy-2-(4-methoxyphenyl)-2,3- dihydro-1,5-benzothiazepin-4(5H)-one 1 * 25 mg

Supplier: LGC Standards PROMOCHEM

(2S,3S)-5-[2-(Dimethylamino)ethyl]-3- hydroxy-2-(4-methoxyphenyl)-2,3- dihydro-1,5-benzothiazepin-4(5H)-one 1 * 25 mg

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Purity: 98% 1 * 25 g

Supplier: MP Biomedicals

Purity: 98% 1 * 25 g

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UN2811III 1 * 50 mg

Supplier: MP Biomedicals

UN2811III 1 * 50 mg

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(2S,3S)-2-(4-Methoxyphenyl)-4-oxo-2,3,4,5- tetrahydro-1,5-benzothiazepin-3-yl Acetate 1 * 25 mg

Supplier: LGC Standards PROMOCHEM

(2S,3S)-2-(4-Methoxyphenyl)-4-oxo-2,3,4,5- tetrahydro-1,5-benzothiazepin-3-yl Acetate 1 * 25 mg

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Atipamezole is an imidazole that potently antagonizes the 2-adrenoceptor (Ki = 1.6 nM).{25705,25706} It shows selectivity over the 1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels.{25706} Th 1 * 50 mg

Supplier: Cayman Chemical

Atipamezole is an imidazole that potently antagonizes the 2-adrenoceptor (Ki = 1.6 nM).{25705,25706} It shows selectivity over the 1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels.{25706} Th 1 * 50 mg

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Rauwolscine is a natural alkaloid that acts as a selective and reversible 2-adregenergic receptor antagonist (Ki = 12 nM).{25653} I t is a stereoisomer of yohimbine, which potently antagonizes both 1- and 2-adrenergic receptors.{25653} Rauwolscine 1 * 100 mg

Supplier: Cayman Chemical

Rauwolscine is a natural alkaloid that acts as a selective and reversible 2-adregenergic receptor antagonist (Ki = 12 nM).{25653} I t is a stereoisomer of yohimbine, which potently antagonizes both 1- and 2-adrenergic receptors.{25653} Rauwolscine 1 * 100 mg

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(2S,3S)-2-(4-Methoxyphenyl)-5-[2-(methylamino)ethyl]-4-oxo-2,3,4 ,5-tetrahydro-1,5-benzothiazepin-3-yl Acetate 1 * 25 mg

Supplier: LGC Standards PROMOCHEM

(2S,3S)-2-(4-Methoxyphenyl)-5-[2-(methylamino)ethyl]-4-oxo-2,3,4 ,5-tetrahydro-1,5-benzothiazepin-3-yl Acetate 1 * 25 mg

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Whi-P180 1 * 1 mg

Supplier: Merck Millipore (Calbiochem‎)

Whi-P180 1 * 1 mg

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Cleaning solution L5104, DURAN® bottle, cleaning solution pepsin/hydrochloric acid 1 * 250 mL

Supplier: SI Analytics

Cleaning solution L5104, DURAN® bottle, cleaning solution pepsin/hydrochloric acid 1 * 250 mL

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Cleaning solution L 510 pepsin/hydrochloric acid 1 * 1 L

Supplier: SI Analytics

Cleaning solution L 510 pepsin/hydrochloric acid 1 * 1 L

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2-(BENZYLMETHYLAMINO)-1-(3-HYDROXYPHENYL 1 * 100 mg

Supplier: LGC Standards PROMOCHEM

2-(BENZYLMETHYLAMINO)-1-(3-HYDROXYPHENYL 1 * 100 mg

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