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Image non disponible-TCIAD0533-25ML

N,N-Diéthyl-p-toluidine ≥98.0% (par GC, analyse par titration)

Numéro de catalogue: (TCIAD0533-25ML)
Fournisseur: TCI
Description: N,N-Diéthyl-p-toluidine ≥98.0% (par GC, analyse par titration)
UOM: 1 * 25 mL
Image non disponible-EHERXA12980100AC

Disulfoton-[diethyl-D10] 100 µg/ml in acetone

Numéro de catalogue: (EHERXA12980100AC)
Fournisseur: EHRENSTORFER
Description: Organic Standard, Disulfoton-[diethyl-D10] 100 µg/ml in acetone, Type de conditionnement: Flacon Verre
UOM: 1 * 1,1 mL
Image non disponible-EHERXA12980100CY

Disulfoton-[diethyl-D10] 100 µg/ml in cyclohexane

Numéro de catalogue: (EHERXA12980100CY)
Fournisseur: EHRENSTORFER
Description: Organic Standard, Disulfoton-[diethyl-D10] 100 µg/ml in cyclohexane, Type de conditionnement: Flacon Verre
UOM: 1 * 1,1 mL
Image non disponible-MOLEM78214946

Benzoate de denatonium

Numéro de catalogue: (MOLEM78214946)
Fournisseur: Molekula
Description: Benzoate de denatonium
UOM: 1 * 5 g

Source d'approvisionnement du marché Il s'agit d'un élément MarketSource. Des frais supplémentaires peuvent s'appliquer.

Image non disponible-TCIAD5295-200MG

Diethyl [2,2'-Bipyridine]-5,5'-dicarboxylate ≥98.0% (par GC, analyse par titration)

Fournisseur: TCI
Description: Diethyl [2,2'-Bipyridine]-5,5'-dicarboxylate ≥98.0% (par GC, analyse par titration)

Image non disponible-BOSSBS-15194R-A350

Anti-C4orf46 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Numéro de catalogue: (BOSSBS-15194R-A350)
Fournisseur: Bioss
Description: Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. The C4orf46 gene product has been provisionally designated C4orf46 pending further characterization.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15193R-A555

Anti-C4orf40 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Numéro de catalogue: (BOSSBS-15193R-A555)
Fournisseur: Bioss
Description: Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. The C4orf40 gene product has been provisionally designated C4orf40 pending further characterization.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15194R-A555

Anti-C4orf46 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Numéro de catalogue: (BOSSBS-15194R-A555)
Fournisseur: Bioss
Description: Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. The C4orf46 gene product has been provisionally designated C4orf46 pending further characterization.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15194R-HRP

Anti-C4orf46 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Numéro de catalogue: (BOSSBS-15194R-HRP)
Fournisseur: Bioss
Description: Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. The C4orf46 gene product has been provisionally designated C4orf46 pending further characterization.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-8251R-A555

Anti-DCUN1D4 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Numéro de catalogue: (BOSSBS-8251R-A555)
Fournisseur: Bioss
Description: The DCN1-like protein family is comprised of Dcun1D1, Dcun1D2, Dcun1D3, Dcun1D4 and Dcun1D5. The founding member, Dcun1D1, is involved in the malignant transformation of squamous cell lineage.Dcun1D4, (defective in cullin neddylation protein 1-like protein 4 or DCN1-like protein 4), also designated KIAA0276, exists as 2 isoforms as a result of alternative splicing and contains one DCUN1 domain. The gene encoding Dcun1D4 maps to chromosome 4, which houses nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-8251R-FITC

Anti-DCUN1D4 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Numéro de catalogue: (BOSSBS-8251R-FITC)
Fournisseur: Bioss
Description: The DCN1-like protein family is comprised of Dcun1D1, Dcun1D2, Dcun1D3, Dcun1D4 and Dcun1D5. The founding member, Dcun1D1, is involved in the malignant transformation of squamous cell lineage.Dcun1D4, (defective in cullin neddylation protein 1-like protein 4 or DCN1-like protein 4), also designated KIAA0276, exists as 2 isoforms as a result of alternative splicing and contains one DCUN1 domain. The gene encoding Dcun1D4 maps to chromosome 4, which houses nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-13180R-A488

Anti-TMA16 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Numéro de catalogue: (BOSSBS-13180R-A488)
Fournisseur: Bioss
Description: Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. The FLJ11184 gene product has been provisionally designated FLJ11184 pending further characterization.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-13366R-A647

Anti-GK2 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Numéro de catalogue: (BOSSBS-13366R-A647)
Fournisseur: Bioss
Description: GK2 is a 553 amino acid protein that belongs to the FGGY kinase family and is involved in the pathway of glycerol degradation. Localized to the outer membrane of the mitochondrion and expressed at high levels in testis, GK2 functions to catalyze the ATP-dependent conversion of glycerol to glycerol 3-phosphate. Via its catalytic activity, GK2 plays an essential role in the regulation of glycerol uptake and metabolism. The gene encoding GK2 maps to chromosome 4, which encodes nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-7687R-CY7

Anti-LAP3 Rabbit Polyclonal Antibody (Cy7®)

Numéro de catalogue: (BOSSBS-7687R-CY7)
Fournisseur: Bioss
Description: LAP3 (leucine aminopeptidase 3), also known as LAPEP or PEPS, is a 519 amino acid protein that localizes to the cytoplasm and belongs to the peptidase M17 family. Existing as a homohexamer, LAP3 uses zinc as a cofactor to catalyze the release of an N-terminal proline from a target peptide and is, therefore, involved in the processing and turnover of intracellular proteins. Multiple isoforms of LAP3 exist due to alternative splicing events. The gene encoding LAP3 maps to human chromosome 4, which houses nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-7687R-CY5.5

Anti-LAP3 Rabbit Polyclonal Antibody (Cy5.5®)

Numéro de catalogue: (BOSSBS-7687R-CY5.5)
Fournisseur: Bioss
Description: LAP3 (leucine aminopeptidase 3), also known as LAPEP or PEPS, is a 519 amino acid protein that localizes to the cytoplasm and belongs to the peptidase M17 family. Existing as a homohexamer, LAP3 uses zinc as a cofactor to catalyze the release of an N-terminal proline from a target peptide and is, therefore, involved in the processing and turnover of intracellular proteins. Multiple isoforms of LAP3 exist due to alternative splicing events. The gene encoding LAP3 maps to human chromosome 4, which houses nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image non disponible-HONC34942-18L

Ether diéthylique, desséché (max. 0.0075% H₂O) stabilisé, Puriss. p.a. ACS, Riedel-de Haën™

Numéro de catalogue: (HONC34942-18L)
Fournisseur: Honeywell Chemicals
Description: Ether diéthylique, desséché (max. 0.0075% H₂O) stabilisé, Puriss. p.a. ACS, Riedel-de Haën™
UOM: 1 * 18 L
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