You Searched For: 2,4-Dichlorophenylboronic+acid


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Supplier: Thermo Scientific
Description: Xylene cyanole FF ∼75% ~75%

Catalog Number: (MOLEM63113303)
Supplier: Molekula
Description: (2,4-Dichlorophenoxy)acetic acid
UOM: 1 * 500 g

Market Source Item This is a MarketSource item. Additional charges may apply

Catalog Number: (APOSBIA0725-250G)
Supplier: APOLLO SCIENTIFIC
Description: L(+)-Asparagine monohydrate ≥99%
UOM: 1 * 250 g


Catalog Number: (BOSSBS-13315R-CY5)
Supplier: Bioss
Description: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 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.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-13315R-CY7)
Supplier: Bioss
Description: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 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.
UOM: 1 * 100 µl


Catalog Number: (ICNA0210155380)
Supplier: MP Biomedicals
Description: 2,4-Dichlorophenoxyacetic acid is a herbicide.
UOM: 1 * 100 g


Catalog Number: (MOLEM38500957)
Supplier: Molekula
Description: 2,4-Bis(trifluoromethyl)benzoic acid
UOM: 1 * 1 g

Market Source Item This is a MarketSource item. Additional charges may apply

Supplier: Alfa Aesar
Description: Xylene cyanole FF ≥70% (dye content)

Catalog Number: (MOLEM71829726)
Supplier: Molekula
Description: Pyridine-2,4-dicarboxylic acid
UOM: 1 * 5 g

Market Source Item This is a MarketSource item. Additional charges may apply

Supplier: Cayman Chemical
Description: Pyridine-2,4-dicarboxylic acid

Supplier: Thermo Scientific
Description: L(+)-Asparagine monohydrate 99%

Catalog Number: (BOSSBS-13315R-A750)
Supplier: Bioss
Description: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 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.
UOM: 1 * 100 µl


Catalog Number: (A8187.0025)
Supplier: PanReac AppliChem
Description: Patent blue V calcium salt ≥85% (by titrimetric analysis)
UOM: 1 * 25 g


Supplier: PanReac AppliChem
Description: L(+)-Asparagine monohydrate

Catalog Number: (MOLE12592063-25G)
Supplier: Molekula
Description: 2,4-Dihydroxy-3,6-dimethylbenzoic acid
UOM: 1 * 25 g

Market Source Item This is a MarketSource item. Additional charges may apply

Catalog Number: (BOSSBS-13315R-HRP)
Supplier: Bioss
Description: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 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.
UOM: 1 * 100 µl


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
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