You Searched For: 3-Fluoro-2-hydroxybenzeneboronic+acid

Catalog Number: (USBI122877)

Supplier: US Biological

Description: Anti-ACO1 Mouse Monoclonal Antibody [clone: 2C1]

UOM: 1 * 100 µG

Supplier: SIGMA ALDRICH MICROSCOPY

Description: 3,3'-Diaminobenzidine tetrahydrochloride hydrate is a chromogen commonly used in immunohistochemistry and other staining techniques to visualise the presence of antigens or antibodies in biological samples. DAB HCl is designed as an immunohistology stain to visualise peroxidase activity in cells. DAB oxidation can be measured using a spectrophotometer.

Catalog Number: (S0252-5G)

Supplier: SIGMA ALDRICH MICROSCOPY

Description: Sulfobromophthalein disodium salt hydrate has been used as a positive control to study the interaction of 11-keto-β-boswellic acid (KBA) and 3-acetyl-11-keto-β-boswellic acid (AKBA) with organic anion transporter OATP1B3.

UOM: 1 * 5 g

Supplier: Alfa Aesar

Description: Gold supplied in 0.1 mg/ml sodium citrate with stabilizer stabilised, nanoparticles 100 nm OD1 (Abs. 572 nm)

Supplier: LGC Standards PROMOCHEM

Description: The solutions are intended for use as a certified reference material or calibration standard for inductively coupled plasma optical emission spectroscopy (ICP-OES), inductively coupled plasma mass spectrometry (ICP-MS), flame or furnace atomic absorption spectroscopy (AA or GFAA), x-ray fluorescence spectroscopy (XRF), and other techniques for elemental analysis.

Supplier: Alfa Aesar

Description: Gold supplied in 0.1 mg/ml sodium citrate with stabilizer stabilised, nanoparticles 50 nm OD1 (Abs. 535 nm)

Supplier: Alfa Aesar

Description: Gold supplied in 0.1 mg/ml sodium citrate with stabilizer stabilised, nanoparticles 40 nm OD1 (Abs. 530 nm)

Supplier: Merck

Description: Silicic acid hydrate, extra pure, precipitated light, Supelco®

Catalog Number: (EDQMY0001028)

Supplier: EDQM

Description: Organic Standard, Esomeprazole magnesium trihydrate, Ph. Eur. standard

UOM: 1 * 5 mg

Supplier: Alfa Aesar

Description: Gold supplied in 0.1 mg/ml sodium citrate with stabilizer stabilised, nanoparticles 80 nm OD1 (Abs. 553 nm)

Catalog Number: (HONC35080-500ML)

Supplier: Honeywell Chemicals

Description: Citrate, pH value: 4.00, 3.994 - 4.006, Reference temperature: 20 °C, Red

UOM: 1 * 500 mL

Supplier: Alfa Aesar

Description: Silver 0,02 mg/ml supplied in 2 mM sodium citrate, nanoparticles 100 nm (Abs. 490 nm)

Catalog Number: (BOSSBS-8228R-A350)

Supplier: Bioss

Description: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-8228R-A647)

Supplier: Bioss

Description: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-8228R-CY3)

Supplier: Bioss

Description: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.

UOM: 1 * 100 µl

Catalog Number: (BOSSBS-8228R-A750)

Supplier: Bioss

Description: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilise calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is also associated with mutations to chromosome 2.

UOM: 1 * 100 µl