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capillary+tubes+fittings
Fournisseur:
HAMMACHER KARL
Description:
Smooth tubing clamps made of stainless steel.
Numéro de catalogue:
(SARS60.540.016)
Fournisseur:
SARSTEDT
Description:
PP, translucent, with assembled integral O-ring screw cap.
UOM:
1 * 500 ST
 Il s'agit d'un élément MarketSource. Des frais supplémentaires peuvent s'appliquer.
Numéro de catalogue:
(201-1620)
Fournisseur:
GLASWARENFABRIK KARL HECHT
Description:
En verre transparent.<B> </B>Deux ampoules et une extension.
UOM:
1 * 1 ST
Fournisseur:
MURRAY, S & CO LTD
Description:
PVC, clear.
Fournisseur:
HIRSCHMANN
Description:
These tubes are biocompatible for sensitive pharmaceuticaland biotechnological applications with good general chemical resistance, excellent resistance to acid, alkali and oxidation, impermeable to light and UV radiation.
Numéro de catalogue:
(LPIT112430)
Fournisseur:
LP ITALIANA SPA
Description:
Stoppers for RIA test tubes, PE, Pour Ø ext.: 11 mm, Pour tubes: 70 mm
UOM:
1 * 12.000 ST
Fournisseur:
Thermo Fisher Scientific
Description:
Pierce™ microcentrifuge tubes are convenient tools for manipulating small volumes of affinity supports for protein purification.
Fournisseur:
GLASWARENFABRIK KARL HECHT
Description:
AR® (soda glass).
Fournisseur:
DELTALAB
Description:
Polyethylene caps for all types of polypropylene and polystyrene tubes.
Fournisseur:
Simport Scientific
Description:
PP. Les parois ultra-fines assurent un transfert thermique rapide et une réduction du temps de cycle et de réaction PCR.
Fournisseur:
SARSTEDT
Description:
PP, translucent or PS, clear.
Numéro de catalogue:
(BOSSBS-9006R-A488)
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-9006R-A555)
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-4100R-A555)
Fournisseur:
Bioss
Description:
Functions in mitochondrial and peroxisomal division. Mediates membrane fission through oligomerization into membrane-associated tubular structures that wrap around the scission site to constrict and sever the mitochondrial membrane through a GTP hydrolysis-dependent mechanism. Through its function in mitochondrial division, ensures the survival of at least some types of postmitotic neurons, including Purkinje cells, by suppressing oxidative damage. Required for normal brain development, including that of cerebellum. Facilitates developmentally regulated apoptosis during neural tube formation. Required for a normal rate of cytochrome c release and caspase activation during apoptosis; this requirement may depend upon the cell type and the physiological apoptotic cues. Also required for mitochondrial fission during mitosis. Required for formation of endocytic vesicles. Proposed to regulate synaptic vesicle membrane dynamics through association with BCL2L1 isoform Bcl-X(L) which stimulates its GTPase activity in synaptic vesicles; the function may require its recruitment by MFF to clathrin-containing vesicles. Required for programmed necrosis execution. Isoform 1 and isoform 4 inhibit peroxisomal division when overexpressed.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-12193R-HRP)
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
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est toujours affiché et vous avez besoin d'aide, s'il vous plaît appelez-nous au 016 385 011
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