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You Searched For: Gold+Germanium+alloy+(88:12+w%)


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Image Unavailable-APOSPC9040-10G

1-Acetyl-5-methyl-3-(trifluoromethyl)pyrazole

Description: 1-Acetyl-5-methyl-3-(trifluoromethyl)pyrazole
Catalog Number: APOSPC9040-10G
UOM: 1 * 10 g
Supplier: APOLLO SCIENTIFIC
Image Unavailable-BLDPBD50010-25G

4-Acetyl-2-chloropyridine 97%

Description: 4-Acetyl-2-chloropyridine 97%
Catalog Number: BLDPBD50010-25G
UOM: 1 * 25 g
Supplier: BLD PHARMATECH GMBH
Image Unavailable-L19235.06

(4-Fluorophenyl)acetyl chloride ≥97%

Description: (4-Fluorophenyl)acetyl chloride ≥97%
Catalog Number: L19235.06
UOM: 1 * 5 g
Supplier: Alfa Aesar
Image Unavailable-BOSSBS-8287R-A647

Anti-DPYS Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Description: Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.
Catalog Number: BOSSBS-8287R-A647
UOM: 1 * 100 µl
Supplier: Bioss
Image Unavailable-BOSSBS-8287R-A350

Anti-DPYS Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Description: Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.
Catalog Number: BOSSBS-8287R-A350
UOM: 1 * 100 µl
Supplier: Bioss
Image Unavailable-B22040.09

DL-Tropic acid ≥98%

Description: DL-Tropic acid ≥98%
Catalog Number: B22040.09
UOM: 1 * 10 g
Supplier: Alfa Aesar
Image Unavailable-92107-50MG

Supelco® Organic Reference Standard, O-Acetyl-ʟ-carnitine hydrochloride

Description: Organic Standard, O-Acetyl-ʟ-carnitine hydrochloride
Catalog Number: 92107-50MG
UOM: 1 * 50 mg
Supplier: Merck
Product Image-ACRO180420050

DL-Valinol 97%

Description: Appearance: Clear yellow Liquid
Catalog Number: ACRO180420050
UOM: 1 * 5 g
Supplier: Thermo Scientific
Image Unavailable-APOSPC4379-250MG

3-Fluoro-DL-tyrosine 97%

Description: 3-Fluoro-DL-tyrosine 97%
Catalog Number: APOSPC4379-250MG
UOM: 1 * 250 mg
Supplier: APOLLO SCIENTIFIC
Image Unavailable-A15054.06

2-Acetyl-3-methylpyrazine ≥98%

Description: 2-Acetyl-3-methylpyrazine ≥98%
Catalog Number: A15054.06
UOM: 1 * 5 g
Supplier: Alfa Aesar
Image Unavailable-BLDPBD32504-5G

2-Iodo-DL-phenylalanine 95%

Description: 2-Iodo-DL-phenylalanine 95%
Catalog Number: BLDPBD32504-5G
UOM: 1 * 5 g
Supplier: BLD PHARMATECH GMBH
Image Unavailable-APOSOR59368-5G

1-Acetyl-5-nitro-1H-indazole

Description: 1-Acetyl-5-nitro-1H-indazole
Catalog Number: APOSOR59368-5G
UOM: 1 * 5 g
Supplier: APOLLO SCIENTIFIC
Image Unavailable-BOSSBS-11822R-A488

Anti-CSAD Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Description: CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Catalog Number: BOSSBS-11822R-A488
UOM: 1 * 100 µl
Supplier: Bioss
Image Unavailable-APOSOR964107-5G

H-DL-Phe(3-CN)-OH 99%

Description: H-DL-Phe(3-CN)-OH 99%
Catalog Number: APOSOR964107-5G
UOM: 1 * 5 g
Supplier: APOLLO SCIENTIFIC
Image Unavailable-APOSOR10821-1G

3-Acetyl-1-(phenylsulphonyl)pyrrole

Description: 3-Acetyl-1-(phenylsulphonyl)pyrrole
Catalog Number: APOSOR10821-1G
UOM: 1 * 1 g
Supplier: APOLLO SCIENTIFIC
Image Unavailable-APOSBIB6077-500MG

Indole-3-acetyl-L-valine

Description: Indole-3-acetyl-L-valine
Catalog Number: APOSBIB6077-500MG
UOM: 1 * 500 mg
Supplier: APOLLO SCIENTIFIC
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