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Puri-Flex®+Precision+Pump+Tubing
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Puri-Flex®+Precision+Pump+Tubing
Fournisseur:
Simport Scientific
Description:
Sterile specimen collection swab.
Fournisseur:
Brand
Description:
En verre AR-Glas®.
Numéro de catalogue:
(ATAGRE-6721)
Fournisseur:
ATAGO
Description:
Accessory for polarimeter, Tube d'observation de 200 mm, 10 ml, Pour: Polax-2L
UOM:
1 * 1 ST
Fournisseur:
DWK Life Sciences
Description:
Modified version for arsine analysis which eliminates the cumbersome ball and socket joint connecting the scrubber and absorber tubes which conforms to ASTM / USP and EPA specifications.
Numéro de catalogue:
(GREI456080_1200)
Fournisseur:
Greiner Bio-One
Description:
Tubes are designed to test trace elements such as aluminium, lead, cadmium, chrome, iron, fluoride, cobalt, copper, lithium, manganese, molybdenum, mercury, selenium, or thallium etc.
UOM:
1 * 1.200 ST
Fournisseur:
IKA
Description:
Agitateurs rotatifs pour un mélange doux mais efficace. Le modèle de base a une vitesse fixe et l'unité numérique propose une vitesse réglable à l'infini. Idéaux pour les échantillons biologiques, en particulier de sang. Adaptés à la séparation et aux processus de mélange d'échantillons en poudre et liquides dans des tubes de 50 ml maximum. Les fixations facilement amovibles permettent un nettoyage rapide en cas d'éclaboussures. Différentes fixations en option permettent d'utiliser les unités pour un grand nombre d'applications.
Fournisseur:
SEMADENI
Description:
LDPE, translucent.
Numéro de catalogue:
(MANA985037)
Fournisseur:
MACHEREY-NAGEL
Description:
A pre-dosed NANOCOLOR® tube test for photometric determination of iron in water.
UOM:
1 * 1 KIT
Numéro de catalogue:
(MANA985014)
Fournisseur:
MACHEREY-NAGEL
Description:
A pre-dosed NANOCOLOR tube test for photometric determination of cadmium in water.
UOM:
1 * 1 KIT
Numéro de catalogue:
(MANA985049)
Fournisseur:
MACHEREY-NAGEL
Description:
A pre-dosed NANOCOLOR® tube test for photometric determination of silver in water.
UOM:
1 * 1 ST
Numéro de catalogue:
(BOSSBS-8153R-A750)
Fournisseur:
Bioss
Description:
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, though 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. The FAM134C gene product has been provisionally designated FAM134C pending further characterisation.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9643R-A647)
Fournisseur:
Bioss
Description:
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.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-8380R-FITC)
Fournisseur:
Bioss
Description:
UBE20, also known as E2-230K, is a 1,292 amino acid member of the uniquitin-conjugating enzyme family that is involved in protein modification. Expressed predominately in heart and skeletal muscle, UBE2O functions to catalyze the ATP-dependent covalent attachment of ubiquitin to select proteins, thereby targeting the ubiquitinated proteins for proteasomal degradation. The gene encoding UBE2O 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. 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, though 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.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9647R-A350)
Fournisseur:
Bioss
Description:
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.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9642R-A555)
Fournisseur:
Bioss
Description:
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.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9640R-A680)
Fournisseur:
Bioss
Description:
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.
UOM:
1 * 100 µl
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