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Image Unavailable-BOSSBS-9639R-CY7

Anti-TEFM Rabbit Polyclonal Antibody (Cy7®)

Descrizione: C17orf42 is a 360 amino acid protein that exists as two alternatively spliced isoforms and is encoded by a gene mapping 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. Tumor suppressor p53 is necessary for maintenance of cellular genetic integrity by moderating cell fate through DNA repair versus cell death. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Like p53, BRCA1 is directly involved in DNA repair, specifically it is recognized as a genetic determinant of early onset breast cancer and predisposition to cancers of the ovary, colon, prostate gland and fallopian tubes. 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 are also associated with chromosome 17.
Codice catalogo: BOSSBS-9639R-CY7
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9639R-CY7
Codice articolo locale: BOSSBS-9639R-CY7
Fornitore: Bioss
Image Unavailable-BOSSBS-9639R-A750

Anti-C17orf42 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Descrizione: C17orf42 is a 360 amino acid protein that exists as two alternatively spliced isoforms and is encoded by a gene mapping to human chromosome 17. Chromosome 17 makes up over 2.5% of the human genome with about 81 million bases encoding over 1200 genes. Two key tumour suppressor genes are associated with chromosome 17, namely, p53 and BRCA1. tumour suppressor p53 is necessary for maintenance of cellular genetic integrity by moderating cell fate through DNA repair versus cell death. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Like p53, BRCA1 is directly involved in DNA repair, specifically it is recognised as a genetic determinant of early onset breast cancer and predisposition to cancers of the ovary, colon, prostate gland and fallopian tubes. Chromosome 17 is also linked to neurofibromatosis, a condition characterised by neural and epidermal lesions, and dysregulated Schwann cell growth. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.
Codice catalogo: BOSSBS-9639R-A750
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9639R-A750
Codice articolo locale: BOSSBS-9639R-A750
Fornitore: Bioss
Image Unavailable-BOSSBS-9639R-A555

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

Descrizione: C17orf42 is a 360 amino acid protein that exists as two alternatively spliced isoforms and is encoded by a gene mapping 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. Tumor suppressor p53 is necessary for maintenance of cellular genetic integrity by moderating cell fate through DNA repair versus cell death. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Like p53, BRCA1 is directly involved in DNA repair, specifically it is recognized as a genetic determinant of early onset breast cancer and predisposition to cancers of the ovary, colon, prostate gland and fallopian tubes. 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 are also associated with chromosome 17.
Codice catalogo: BOSSBS-9639R-A555
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9639R-A555
Codice articolo locale: BOSSBS-9639R-A555
Fornitore: Bioss
Product Image-ACRO229090250

Lithocholic acid 98%

Descrizione: Lithocholic acid 98%
Codice catalogo: ACRO229090250
UOM: 1 * 25 g
Codice articolo fornitore: 229090250
Codice articolo locale: ACRO229090250
Fornitore: Thermo Fisher Scientific

MSDS


Image Unavailable-BOSSBS-13685R-A750

Anti-C17orf87 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Descrizione: C17orf87 (chromosome 17 open reading frame 87) is a 145 amino acid protein that is encoded by a gene mapping 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. Tumor suppressor p53 is necessary for maintenance of cellular genetic integrity by moderating cell fate through DNA repair versus cell death. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Like p53, BRCA1 is directly involved in DNA repair, specifically it is recognized as a genetic determinant of early onset breast cancer and predisposition to cancers of the ovary, colon, prostate gland and fallopian tubes. 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 are also associated with chromosome 17.
Codice catalogo: BOSSBS-13685R-A750
UOM: 1 * 100 µl
Codice articolo fornitore: BS-13685R-A750
Codice articolo locale: BOSSBS-13685R-A750
Fornitore: Bioss
Image Unavailable-BOSSBS-13685R-A488

Anti-C17orf87 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Descrizione: C17orf87 (chromosome 17 open reading frame 87) is a 145 amino acid protein that is encoded by a gene mapping 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. Tumor suppressor p53 is necessary for maintenance of cellular genetic integrity by moderating cell fate through DNA repair versus cell death. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Like p53, BRCA1 is directly involved in DNA repair, specifically it is recognized as a genetic determinant of early onset breast cancer and predisposition to cancers of the ovary, colon, prostate gland and fallopian tubes. 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 are also associated with chromosome 17.
Codice catalogo: BOSSBS-13685R-A488
UOM: 1 * 100 µl
Codice articolo fornitore: BS-13685R-A488
Codice articolo locale: BOSSBS-13685R-A488
Fornitore: Bioss
Image Unavailable-BOSSBS-6578R-HRP

Anti-SAMD14 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Descrizione: 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.
Codice catalogo: BOSSBS-6578R-HRP
UOM: 1 * 100 µl
Codice articolo fornitore: BS-6578R-HRP
Codice articolo locale: BOSSBS-6578R-HRP
Fornitore: Bioss
Image Unavailable-BOSSBS-6578R-FITC

Anti-SAMD14 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Descrizione: 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.
Codice catalogo: BOSSBS-6578R-FITC
UOM: 1 * 100 µl
Codice articolo fornitore: BS-6578R-FITC
Codice articolo locale: BOSSBS-6578R-FITC
Fornitore: Bioss
Image Unavailable-APOSBICR124-1G

(R)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoic acid

Descrizione: (R)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoic acid
Codice catalogo: APOSBICR124-1G
UOM: 1 * 1 g
Codice articolo fornitore: BICR124-1G
Codice articolo locale: APOSBICR124-1G
Fornitore: Apollo Scientific
Image Unavailable-BOSSBS-9557R-A488

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

Descrizione: 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.
Codice catalogo: BOSSBS-9557R-A488
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9557R-A488
Codice articolo locale: BOSSBS-9557R-A488
Fornitore: Bioss
Image Unavailable-BOSSBS-9557R-A680

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

Descrizione: 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.
Codice catalogo: BOSSBS-9557R-A680
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9557R-A680
Codice articolo locale: BOSSBS-9557R-A680
Fornitore: Bioss
Image Unavailable-BOSSBS-9557R-A555

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

Descrizione: 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.
Codice catalogo: BOSSBS-9557R-A555
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9557R-A555
Codice articolo locale: BOSSBS-9557R-A555
Fornitore: Bioss
Product Image-BOSSBS-6578R

Anti-SAMD14 Rabbit Polyclonal Antibody

Descrizione: 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.
Codice catalogo: BOSSBS-6578R
UOM: 1 * 100 µl
Codice articolo fornitore: BS-6578R
Codice articolo locale: BOSSBS-6578R
Fornitore: Bioss
Image Unavailable-TCIAM2465-1G

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

Descrizione: Methyl-5-methylpyrazole-3-carboxylate ≥98.0% (by GC)
Codice catalogo: TCIAM2465-1G
UOM: 1 * 1 g
Codice articolo fornitore: M2465-1G
Codice articolo locale: TCIAM2465-1G
Fornitore: TCI
Image Unavailable-TCIAS0928-500G

DL-Sodium lactate 60% in water

Descrizione: DL-Sodium lactate 60% in water
Codice catalogo: TCIAS0928-500G
UOM: 1 * 500 g
Codice articolo fornitore: S0928-500G
Codice articolo locale: TCIAS0928-500G
Fornitore: TCI

Certificati


Image Unavailable-BOSSBS-9557R-A750

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

Descrizione: 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.
Codice catalogo: BOSSBS-9557R-A750
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9557R-A750
Codice articolo locale: BOSSBS-9557R-A750
Fornitore: Bioss
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