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Puri-Flex®+Precision+Pump+Tubing
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Puri-Flex®+Precision+Pump+Tubing
Fournisseur:
KARTELL
Description:
En PS, expansé, blanc.
Fournisseur:
Bel-Art Products, a Part of SP
Description:
PP gas sampling bulbs have PP stopcocks with free-turning Teflon® PTFE plugs.
Fournisseur:
HAMMACHER KARL
Description:
Smooth tubing clamps made of stainless steel.
Fournisseur:
MURRAY, S & CO LTD
Description:
PVC, clear.
Fournisseur:
VWR Collection
Description:
<B>Refroidisseur de laboratoire mini −20 °C PC, gel non toxique </B>Le mini refroidisseur de laboratoire à −20 °C contient 12 tubes de microcentrifugeuse de 0,5 ou 1,5 ml à une température inférieure à −20 °C pendant plus d'une heure. Idéal pour une utilisation sur paillasse ou pour le transport. Rempli de gel non toxique. Avant utilisation, placer au congélateur à –25 °C pendant au moins 24 heures, conserver à –25 °C entre les utilisations.
Numéro de catalogue:
(TIGV383440G)
Fournisseur:
TIGER-VAC
Description:
Transfer tubing, Suction hose, noir, Longueur: 3 m
UOM:
1 * 1 ST
New Product
Fournisseur:
DWK Life Sciences
Description:
Manufactured from 51 expansion borosilicate glass that conforms to ASTM Type I, Class B and USP Type I requirements.
Fournisseur:
Greiner Bio-One
Description:
Bouchons crénelés pour tubes, Grip stopper, PE, Couleur: naturel, Pour tubes: 16 - 16,5 mm O.D.
Numéro de catalogue:
(BOSSBS-9006R-A750)
Fournisseur:
Bioss
Description:
Adenosine deaminase is an enzyme that is present in most tissues and exists predominantly as a monomer, although in some tissues it is associated with adenosine deaminase-binding protein. Adenosine deaminase degrades extracellular adenosine, which is toxic for lymphocytes. A novel family of growth factors that share sequence similarity to adenosine deaminase has been identified. The cat eye syndrome critical region protein (CECR) family includes CECR1, CECR2, CECR3, CECR4, CECR5, CECR6, CECR7, CECR8 and CECR9. The genes encoding CECR proteins are candidates for Cat Eye Syndrome (CES), a developmental disorder associated with the duplication of a 2 Mb region of 22q11.2. CES is characterised by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. CECR family members are widely expressed. Specifically, CECR1 has the highest expression in adult heart, lung, lymphoblasts and placenta. CECR2 is also involved in neurulation and chromatin remodeling. Mutations in the CECR2 gene result in neural tube defects.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9006R-FITC)
Fournisseur:
Bioss
Description:
Adenosine deaminase is an enzyme that is present in most tissues and exists predominantly as a monomer, although in some tissues it is associated with adenosine deaminase-binding protein. Adenosine deaminase degrades extracellular adenosine, which is toxic for lymphocytes. A novel family of growth factors that share sequence similarity to adenosine deaminase has been identified. The cat eye syndrome critical region protein (CECR) family includes CECR1, CECR2, CECR3, CECR4, CECR5, CECR6, CECR7, CECR8 and CECR9. The genes encoding CECR proteins are candidates for Cat Eye Syndrome (CES), a developmental disorder associated with the duplication of a 2 Mb region of 22q11.2. CES is characterized by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. CECR family members are widely expressed. Specifically, CECR1 has the highest expression in adult heart, lung, lymphoblasts and placenta. CECR2 is also involved in neurulation and chromatin remodeling. Mutations in the CECR2 gene result in neural tube defects.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-12193R-A350)
Fournisseur:
Bioss
Description:
Transcription factor required for formation of positional identity in the developing retina, regionalization of the optic chiasm and morphogenesis of the kidney. Can neuralize ectodermal cells directly By similarity. Binds to the consensus sequence 5'-A[AT]T[AG]TTTGTTT-3' and acts as a transcriptional repressor. Also acts as a transcriptional activator. Promotes development of neural crest cells from neural tube progenitors. Restricts neural progenitor cells to the neural crest lineage while suppressing interneuron differentiation. Required for maintenance of pluripotent cells in the pre-implantation and peri-implantation stages of embryogenesis. Probable transcription factor involved in embryogenesis and somatogenesis. FOXD1 is involved in regulating inflammation as well as kidney and retinal development. FOXD1 regulates the activity of NFAT and NFkB. Deficiency of FOXD1 results in multiorgan systemic inflammation, exaggerated Th cell-derived cytokine production, and T cell proliferation in autogolgous MLRs. In kidneys, FOXD1 controls the production of signals required for the normal transition of induced mesenchyme into tubular epithelium and full growth and branching of the collecting system. Deletion of FOXD1 results in renal abnormalities. FOXD2 acts as a modulator of T cell activation.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-13685R-HRP)
Fournisseur:
Bioss
Description:
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
Fournisseur:
BOCHEM
Description:
Rack, made of stainless steel 18/10.
Fournisseur:
ADELPHI MANUFACTURING
Description:
Accessories for Plastic and Laminate Tube Sealer, Vesta 1C
Fournisseur:
DWK Life Sciences
Description:
Ces tubes de distribution de gaz sont conçus pour les réactions entre les gaz et les liquides. Ils sont fabriqués en verre borosilicaté 3.3 DURAN® transparent.
Fournisseur:
LAUDA
Description:
Rack, Test tube, Stainless steel rack for 1×in AL 5, 3×in AL 12, 5×in AL 18, AL 25, Pour tubes Ø: 24/30 mm, Nb de places: 10, Pour tubes: 110 mm high
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