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Image Unavailable-BOSSBS-13325R-A750

Anti-GDPD1/GDE4 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Descrizione: 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.
Codice catalogo: BOSSBS-13325R-A750
UOM: 1 * 100 µl
Codice articolo fornitore: BS-13325R-A750
Codice articolo locale: BOSSBS-13325R-A750
Fornitore: Bioss
Image Unavailable-BOSSBS-9647R-A350

Anti-C17ORF77 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Descrizione: C17orf77 is a 243 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-9647R-A350
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9647R-A350
Codice articolo locale: BOSSBS-9647R-A350
Fornitore: Bioss
Image Unavailable-BOSSBS-9643R-A647

Anti-C17ORF64 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Descrizione: C17orf64 is a 562 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-9643R-A647
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9643R-A647
Codice articolo locale: BOSSBS-9643R-A647
Fornitore: Bioss
Image Unavailable-BOSSBS-9647R-CY5.5

Anti-C17ORF77 Rabbit Polyclonal Antibody (Cy5.5®)

Descrizione: C17orf77 is a 243 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-9647R-CY5.5
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9647R-CY5.5
Codice articolo locale: BOSSBS-9647R-CY5.5
Fornitore: Bioss
Image Unavailable-BOSSBS-9640R-A680

Anti-C17orf49 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Descrizione: C17orf49 is a 172 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 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-9640R-A680
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9640R-A680
Codice articolo locale: BOSSBS-9640R-A680
Fornitore: Bioss
Image Unavailable-BOSSBS-9642R-A555

Anti-EFCAB13 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Descrizione: C17orf57 is a 973 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-9642R-A555
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9642R-A555
Codice articolo locale: BOSSBS-9642R-A555
Fornitore: Bioss
Image Unavailable-BOSSBS-9639R-A350

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

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-A350
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9639R-A350
Codice articolo locale: BOSSBS-9639R-A350
Fornitore: Bioss
Image Unavailable-BOSSBS-9639R-FITC

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

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-FITC
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9639R-FITC
Codice articolo locale: BOSSBS-9639R-FITC
Fornitore: Bioss
Image Unavailable-BOSSBS-6578R-A680

Anti-SAMD14 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

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 characterised by neural and epidermal lesions, and dysregulated Schwann cell growth, Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease.
Codice catalogo: BOSSBS-6578R-A680
UOM: 1 * 100 µl
Codice articolo fornitore: BS-6578R-A680
Codice articolo locale: BOSSBS-6578R-A680
Fornitore: Bioss
Product Image-521-1108

Rotori per centrifughe Pico™ e Fresco™

Descrizione: Increase nucleic acid sample separation by using the Thermo Scientific™ 10×5 ml rotor with ClickSeal™ biocontainment lid.
Codice catalogo: 521-1108
UOM: 1 * 1 pezzi
Codice articolo fornitore: 75003473
Codice articolo locale: HERA75003473
Fornitore: Thermo Scientific
Image Unavailable-BOSSBS-13685R-A350

Anti-C17orf87 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

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-A350
UOM: 1 * 100 µl
Codice articolo fornitore: BS-13685R-A350
Codice articolo locale: BOSSBS-13685R-A350
Fornitore: Bioss
Image Unavailable-H62473.03

(R)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoic acid 95%

Descrizione: (R)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoic acid 95%
Codice catalogo: H62473.03
UOM: 1 * 1 g
Codice articolo fornitore: H62473.03
Codice articolo locale: ALFAH62473.03
Fornitore: Thermo Fisher Scientific

Certificati


Image Unavailable-APOSOR307074-500G

Boc-D-Pro-OH 97%

Descrizione: Boc-D-Pro-OH 97%
Codice catalogo: APOSOR307074-500G
UOM: 1 * 500 g
Codice articolo fornitore: OR307074-500G
Codice articolo locale: APOSOR307074-500G
Fornitore: Apollo Scientific
Image Unavailable-BOSSBS-9640R-CY3

Anti-C17ORF49 Rabbit Polyclonal Antibody (Cy3®)

Descrizione: C17orf49 is a 172 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-9640R-CY3
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9640R-CY3
Codice articolo locale: BOSSBS-9640R-CY3
Fornitore: Bioss
Image Unavailable-BOSSBS-9641R-A555

Anti-C17ORF53 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Descrizione: C17orf53 is a 647 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-9641R-A555
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9641R-A555
Codice articolo locale: BOSSBS-9641R-A555
Fornitore: Bioss
Image Unavailable-BOSSBS-9646R-A350

Anti-C17ORF75 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Descrizione: C17orf75 is a 396 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-9646R-A350
UOM: 1 * 100 µl
Codice articolo fornitore: BS-9646R-A350
Codice articolo locale: BOSSBS-9646R-A350
Fornitore: Bioss
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