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Image du produit-ACRO444930050

2,4-Dimethoxy-5-pyrimidineboronic acid pinacol ester 97%

Fournisseur: Thermo Fisher Scientific
Description: 2,4-Dimethoxy-5-pyrimidineboronic acid pinacol ester 97%

MSMD

Image du produit-ACRO148141000

Acide 3α,12α-dihydroxy-5β-cholane-24-oïque 98.5%

Fournisseur: Thermo Fisher Scientific
Description: Acide 3α,12α-dihydroxy-5β-cholane-24-oïque 98.5%

MSMD

Image non disponible-TCIAB2977-25G

Hydrogéno-(R)-pyrrolidine-1,2-dicarboxylate de 1-(tert-butyle) ≥98.0% (par HPLC, analyse par titration)

Fournisseur: TCI
Description: Hydrogéno-(R)-pyrrolidine-1,2-dicarboxylate de 1-(tert-butyle) ≥98.0% (par HPLC, analyse par titration)

Image non disponible-TCIAM2465-1G

Methyl-5-methylpyrazole-3-carboxylate ≥98.0% (par GC)

Fournisseur: TCI
Description: Methyl-5-methylpyrazole-3-carboxylate ≥98.0% (par GC)

Image non disponible-BOSSBS-9557R-A488

Anti-GLTPD2 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Numéro de catalogue: (BOSSBS-9557R-A488)
Fournisseur: Bioss
Description: The GLTP (glycolipid transfer protein) superfamily is defined by a unique lipid transfer/binding fold (GLTP fold) that accelerate glycolipid intermembrane transfer. GLTPD2 is a 291 amino acid protein that belongs to the GLTP family. The gene encoding GLTPD2 maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, p53 and BRCA1. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth are both linked to mutations on chromosome 17. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-9557R-A680

Anti-GLTPD2 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Numéro de catalogue: (BOSSBS-9557R-A680)
Fournisseur: Bioss
Description: The GLTP (glycolipid transfer protein) superfamily is defined by a unique lipid transfer/binding fold (GLTP fold) that accelerate glycolipid intermembrane transfer. GLTPD2 is a 291 amino acid protein that belongs to the GLTP family. The gene encoding GLTPD2 maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1200 genes. Two key tumour suppressor genes are associated with chromosome 17, p53 and BRCA1. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Neurofibromatosis, a condition characterised by neural and epidermal lesions, and dysregulated Schwann cell growth are both linked to mutations on chromosome 17. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-9557R-A555

Anti-GLTPD2 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Numéro de catalogue: (BOSSBS-9557R-A555)
Fournisseur: Bioss
Description: The GLTP (glycolipid transfer protein) superfamily is defined by a unique lipid transfer/binding fold (GLTP fold) that accelerate glycolipid intermembrane transfer. GLTPD2 is a 291 amino acid protein that belongs to the GLTP family. The gene encoding GLTPD2 maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, p53 and BRCA1. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth are both linked to mutations on chromosome 17. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-9557R-CY5.5

Anti-GLTPD2 Rabbit Polyclonal Antibody (Cy5.5®)

Numéro de catalogue: (BOSSBS-9557R-CY5.5)
Fournisseur: Bioss
Description: The GLTP (glycolipid transfer protein) superfamily is defined by a unique lipid transfer/binding fold (GLTP fold) that accelerate glycolipid intermembrane transfer. GLTPD2 is a 291 amino acid protein that belongs to the GLTP family. The gene encoding GLTPD2 maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, p53 and BRCA1. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth are both linked to mutations on chromosome 17. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-9557R-CY5

Anti-GLTPD2 Rabbit Polyclonal Antibody (Cy5®)

Numéro de catalogue: (BOSSBS-9557R-CY5)
Fournisseur: Bioss
Description: The GLTP (glycolipid transfer protein) superfamily is defined by a unique lipid transfer/binding fold (GLTP fold) that accelerate glycolipid intermembrane transfer. GLTPD2 is a 291 amino acid protein that belongs to the GLTP family. The gene encoding GLTPD2 maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, p53 and BRCA1. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth are both linked to mutations on chromosome 17. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.
UOM: 1 * 100 µl
Image du produit-BOSSBS-6578R

Anti-SAMD14 Rabbit Polyclonal Antibody

Numéro de catalogue: (BOSSBS-6578R)
Fournisseur: Bioss
Description: The sterile alpha motif (SAM) domain is a 70 residue structure found in a large number of proteins involved in diverse processes present throughout eukaryotes. The SAM domain is known to bind RNA and is arranged in a small five-helix bundle with two large interfaces. SAMD14 (sterile alpha motif domain-containing protein 14) is a 417 amino acid protein encoded by the SAMD14 gene which maps to human chromosome 17. Chromosome 17 makes up over 2.5% of the human genome with about 81 million bases encoding over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1. Chromosome 17 is also linked to neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth, Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease.
UOM: 1 * 100 µl
Image non disponible-APOSOR925263-5G

Acide trans,trans-buta-1,3-diène-1,4-dicarboxylique 95%

Fournisseur: Apollo Scientific
Description: Acide trans,trans-buta-1,3-diène-1,4-dicarboxylique 95%

Image non disponible-BOSSBS-13325R-A350

Anti-GDPD1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Numéro de catalogue: (BOSSBS-13325R-A350)
Fournisseur: Bioss
Description: GDE4 is a 314 amino acid cytoplasmic and multi-pass membrane protein that belongs to the glycerophosphoryl diester phosphodiesterase family. Expressed in small intestine, placenta, kidney, ovary, thymus, pancreas, spleen, liver and peripheral blood leukocytes, GDE4 contains one GDPD domain and exists as three alternatively spliced isoforms. GDE4 is encoded by a gene that maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-13325R-A555

Anti-GDPD1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Numéro de catalogue: (BOSSBS-13325R-A555)
Fournisseur: Bioss
Description: GDE4 is a 314 amino acid cytoplasmic and multi-pass membrane protein that belongs to the glycerophosphoryl diester phosphodiesterase family. Expressed in small intestine, placenta, kidney, ovary, thymus, pancreas, spleen, liver and peripheral blood leukocytes, GDE4 contains one GDPD domain and exists as three alternatively spliced isoforms. GDE4 is encoded by a gene that maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-9557R-CY3

Anti-GLTPD2 Rabbit Polyclonal Antibody (Cy3®)

Numéro de catalogue: (BOSSBS-9557R-CY3)
Fournisseur: Bioss
Description: The GLTP (glycolipid transfer protein) superfamily is defined by a unique lipid transfer/binding fold (GLTP fold) that accelerate glycolipid intermembrane transfer. GLTPD2 is a 291 amino acid protein that belongs to the GLTP family. The gene encoding GLTPD2 maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, p53 and BRCA1. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth are both linked to mutations on chromosome 17. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-9557R-A750

Anti-GLTPD2 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Numéro de catalogue: (BOSSBS-9557R-A750)
Fournisseur: Bioss
Description: The GLTP (glycolipid transfer protein) superfamily is defined by a unique lipid transfer/binding fold (GLTP fold) that accelerate glycolipid intermembrane transfer. GLTPD2 is a 291 amino acid protein that belongs to the GLTP family. The gene encoding GLTPD2 maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1200 genes. Two key tumour suppressor genes are associated with chromosome 17, p53 and BRCA1. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Neurofibromatosis, a condition characterised by neural and epidermal lesions, and dysregulated Schwann cell growth are both linked to mutations on chromosome 17. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.
UOM: 1 * 100 µl
Image non disponible-TCIAC0315-100G

Acide 3α,12α-dihydroxy-5β-cholane-24-oïque ≥98.0% (par GC, analyse par titration)

Fournisseur: TCI
Description: Acide 3α,12α-dihydroxy-5β-cholane-24-oïque ≥98.0% (par GC, analyse par titration)

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Le stock de cet article est limité mais peut être disponible dans un entrepôt proche de vous. Merci de vous assurer que vous êtes connecté sur le site afin que le stock disponible soit affiché. Si l'call est toujours affiché et vous avez besoin d'aide, s'il vous plaît appelez-nous au 016 385 011
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