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Image Unavailable-BOSSBS-13325R-A488

Anti-GDPD1 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Codice catalogo: (BOSSBS-13325R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-13325R-A488
Codice articolo locale: BOSSBS-13325R-A488
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13325R-CY7

Anti-GDPD1 Rabbit Polyclonal Antibody (Cy7®)

Codice catalogo: (BOSSBS-13325R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-13325R-CY7
Codice articolo locale: BOSSBS-13325R-CY7
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13325R-FITC

Anti-GDPD1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Codice catalogo: (BOSSBS-13325R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-13325R-FITC
Codice articolo locale: BOSSBS-13325R-FITC
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13325R-A680

Anti-GDPD1/GDE4 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Codice catalogo: (BOSSBS-13325R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-13325R-A680
Codice articolo locale: BOSSBS-13325R-A680
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-6578R-CY5.5

Anti-SAMD14 Rabbit Polyclonal Antibody (Cy5.5®)

Codice catalogo: (BOSSBS-6578R-CY5.5)
Fornitore: Bioss
Codice articolo fornitore: BS-6578R-CY5.5
Codice articolo locale: BOSSBS-6578R-CY5.5
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-6578R-CY7

Anti-SAMD14 Rabbit Polyclonal Antibody (Cy7®)

Codice catalogo: (BOSSBS-6578R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-6578R-CY7
Codice articolo locale: BOSSBS-6578R-CY7
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9557R-A750

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

Codice catalogo: (BOSSBS-9557R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-9557R-A750
Codice articolo locale: BOSSBS-9557R-A750
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.
UOM: 1 * 100 µl
Image Unavailable-APOSOR312205-250MG

tert-Butyl 2,6-diazaspiro[3.5]nonane-6-carboxylate

Codice catalogo: (APOSOR312205-250MG)
Fornitore: Apollo Scientific
Codice articolo fornitore: OR312205-250MG
Codice articolo locale: APOSOR312205-250MG
Descrizione: tert-Butyl 2,6-diazaspiro[3.5]nonane-6-carboxylate
UOM: 1 * 250 mg
Image Unavailable-BOSSBS-6578R-CY3

Anti-SAMD14 Rabbit Polyclonal Antibody (Cy3®)

Codice catalogo: (BOSSBS-6578R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-6578R-CY3
Codice articolo locale: BOSSBS-6578R-CY3
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13685R-CY7

Anti-C17orf87 Rabbit Polyclonal Antibody (Cy7®)

Codice catalogo: (BOSSBS-13685R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-13685R-CY7
Codice articolo locale: BOSSBS-13685R-CY7
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.
UOM: 1 * 100 µl
Image Unavailable-TCIAS0836-5G

Sodium-2,3,5,6-tetrafluoro-4-hydroxybenzenesulphonate ≥98.0% (by HPLC)

Fornitore: TCI
Descrizione: Sodium-2,3,5,6-tetrafluoro-4-hydroxybenzenesulphonate ≥98.0% (by HPLC)

Image Unavailable-TCIAI0471-1G

Methyl (2S,3S)-2-isocyanato-3-methylvalerate ≥98.0% (by GC)

Fornitore: TCI
Descrizione: Methyl (2S,3S)-2-isocyanato-3-methylvalerate ≥98.0% (by GC)

Image Unavailable-BOSSBS-9557R-A488

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

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

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

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

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

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

Anti-SAMD14 Rabbit Polyclonal Antibody

Codice catalogo: (BOSSBS-6578R)
Fornitore: Bioss
Codice articolo fornitore: BS-6578R
Codice articolo locale: BOSSBS-6578R
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.
UOM: 1 * 100 µl
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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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