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Fournisseur: RATIOLAB
Description: Bags of very strong PP-film with a broad seam at the bottom, for the disposal of contaminated labware.

Numéro de catalogue: (VERN20-F)
Fournisseur: Saint Gobain Life Sciences
Description: KryoSure® Cryopreservation bags safely freeze and protect biologics at temperatures down to, and even beyond, liquid nitrogen temperatures (–196 °C). All KryoSure® bags are made from the highest quality USP Class VI Fluorinated Ethylene Propylene (FEP) material.
UOM: 1 * 1 ST

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Fournisseur: Roth Carl
Description: These free-standing sample bags specially formed base allows bags to stand completely free and without support and are suitable for liquids and solids.

Fournisseur: JOUAN
Description: Liner for 550 ml Quin/Quad blood bags with 1 partition, Pour: Thermo Scientific Jouan KR4i

Fournisseur: Alpha Packaging
Description: Sacs jaunes en polyéthylène non-autoclavables. Livrés dans des distributeurs.
En PE, épaisseur 62,5 µm (gauge 250).

Fournisseur: INTERSCIENCE
Description: These non-filter sample preparation bags are ideal for homogenising samples.
Fournisseur: DELTA T
Description: BlueLine Bags are economical and durable. Its insulating property ensures the maintainance of constant internal temperature and protects the samples against heat or cold environment.

Fournisseur: Corning
Description: Rocker cell culture bags are designed for use with commercial rocking motion bioreactor chambers, and feature irradiated ethylene vinyl acetate (EVA)/low-density polyethylene (ULDPE) 9101 film and stability bars on each side. These sterile, single-use cell culture bags are ideal for applications from basic research to large-scale biopharmaceutical manufacturing.
Fournisseur: Bel-Art Products, a Part of SP
Description: Bright red, autoclavable bags feature one long flap for easy opening. Printed with the biohazard symbol and sterilization indicator patch, they are made of High Molecular Weight, High-Density (HMHD) polyethylene.
Numéro de catalogue: (BOSSBS-13647R)
Fournisseur: Bioss
Description: c-Jun NH2-terminal kinases (JNKs) are distant members of the MAP kinase family (1). JNK1 is activated by dual phosphorylation at a Thr-Pro-Tyr motif in response to ultraviolet (UV) light, and it functions to phosphorylate c-Jun at amino terminal serine regulatory sites, Ser-63 and Ser-73, resulting in transcriptional activation (2-5). Two additional JNK family members have been identified as JNK2 and JNK3 (3). JIP-1 (for JNK interacting protein-1) has been identified as a cytoplasmic inhibitor of JNK that retains JNK in the cytoplasm, thereby inhibiting JNK-regulated gene expression. Evidence suggests that JNK1 and JNK2 bind to JIP-1 with greater affinity than to ATF-2 and c-Jun, which are targets of the JNK signaling pathway. JIP-1 contains an amino terminal JNK binding domain and a carboxy terminal SH3 domain. ATF-2 and c-Jun also contain the JNK binding domain and are thought to compete with JIP-1 for JNK binding (6). Multiple splice variants if JIP-1, including JIP-1b, JIP-1c (also designated islet-brain 1 or IB-1), JIP-2a, JIP-2b and JIP-3, have been identified in brain (7).
UOM: 1 * 100 µl


Numéro de catalogue: (BOSSBS-13647R-A647)
Fournisseur: Bioss
Description: c-Jun NH2-terminal kinases (JNKs) are distant members of the MAP kinase family (1). JNK1 is activated by dual phosphorylation at a Thr-Pro-Tyr motif in response to ultraviolet (UV) light, and it functions to phosphorylate c-Jun at amino terminal serine regulatory sites, Ser-63 and Ser-73, resulting in transcriptional activation (2-5). Two additional JNK family members have been identified as JNK2 and JNK3 (3). JIP-1 (for JNK interacting protein-1) has been identified as a cytoplasmic inhibitor of JNK that retains JNK in the cytoplasm, thereby inhibiting JNK-regulated gene expression. Evidence suggests that JNK1 and JNK2 bind to JIP-1 with greater affinity than to ATF-2 and c-Jun, which are targets of the JNK signaling pathway. JIP-1 contains an amino terminal JNK binding domain and a carboxy terminal SH3 domain. ATF-2 and c-Jun also contain the JNK binding domain and are thought to compete with JIP-1 for JNK binding (6). Multiple splice variants if JIP-1, including JIP-1b, JIP-1c (also designated islet-brain 1 or IB-1), JIP-2a, JIP-2b and JIP-3, have been identified in brain (7).
UOM: 1 * 100 µl


Numéro de catalogue: (BOSSBS-13647R-A350)
Fournisseur: Bioss
Description: c-Jun NH2-terminal kinases (JNKs) are distant members of the MAP kinase family (1). JNK1 is activated by dual phosphorylation at a Thr-Pro-Tyr motif in response to ultraviolet (UV) light, and it functions to phosphorylate c-Jun at amino terminal serine regulatory sites, Ser-63 and Ser-73, resulting in transcriptional activation (2-5). Two additional JNK family members have been identified as JNK2 and JNK3 (3). JIP-1 (for JNK interacting protein-1) has been identified as a cytoplasmic inhibitor of JNK that retains JNK in the cytoplasm, thereby inhibiting JNK-regulated gene expression. Evidence suggests that JNK1 and JNK2 bind to JIP-1 with greater affinity than to ATF-2 and c-Jun, which are targets of the JNK signaling pathway. JIP-1 contains an amino terminal JNK binding domain and a carboxy terminal SH3 domain. ATF-2 and c-Jun also contain the JNK binding domain and are thought to compete with JIP-1 for JNK binding (6). Multiple splice variants if JIP-1, including JIP-1b, JIP-1c (also designated islet-brain 1 or IB-1), JIP-2a, JIP-2b and JIP-3, have been identified in brain (7).
UOM: 1 * 100 µl


Numéro de catalogue: (BOSSBS-13647R-CY5)
Fournisseur: Bioss
Description: c-Jun NH2-terminal kinases (JNKs) are distant members of the MAP kinase family (1). JNK1 is activated by dual phosphorylation at a Thr-Pro-Tyr motif in response to ultraviolet (UV) light, and it functions to phosphorylate c-Jun at amino terminal serine regulatory sites, Ser-63 and Ser-73, resulting in transcriptional activation (2-5). Two additional JNK family members have been identified as JNK2 and JNK3 (3). JIP-1 (for JNK interacting protein-1) has been identified as a cytoplasmic inhibitor of JNK that retains JNK in the cytoplasm, thereby inhibiting JNK-regulated gene expression. Evidence suggests that JNK1 and JNK2 bind to JIP-1 with greater affinity than to ATF-2 and c-Jun, which are targets of the JNK signaling pathway. JIP-1 contains an amino terminal JNK binding domain and a carboxy terminal SH3 domain. ATF-2 and c-Jun also contain the JNK binding domain and are thought to compete with JIP-1 for JNK binding (6). Multiple splice variants if JIP-1, including JIP-1b, JIP-1c (also designated islet-brain 1 or IB-1), JIP-2a, JIP-2b and JIP-3, have been identified in brain (7).
UOM: 1 * 100 µl


Fournisseur: Sampling Systems
Description: Boîtier d'échantillonneurs supérieur, verrouillable, avec charnières métalliques, 870×285×116 mm

Fournisseur: Bel-Art Products, a Part of SP
Description: Bags, in PP, 38 or 50 µm thick, orange, with 'Biohazard' symbol.

Fournisseur: BURKLE
Description: Bags with the patented zipper are for ideal for storing, collecting, protecting and shipping of specimens, samples and sales products.

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