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Masterflex+Single-use+Flow+Sensor


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Numéro de catalogue: (BOSSBS-5221R-CY5.5)

Fournisseur:  Bioss
Description:   This gene encodes a nuclear phosphoprotein that plays a role in maintaining genomic stability, and it also acts as a tumor suppressor. The encoded protein combines with other tumor suppressors, DNA damage sensors, and signal transducers to form a large multi-subunit protein complex known as the BRCA1-associated genome surveillance complex (BASC). This gene product associates with RNA polymerase II, and through the C-terminal domain, also interacts with histone deacetylase complexes. This protein thus plays a role in transcription, DNA repair of double-stranded breaks, and recombination. Mutations in this gene are responsible for approximately 40% of inherited breast cancers and more than 80% of inherited breast and ovarian cancers. Alternative splicing plays a role in modulating the subcellular localization and physiological function of this gene. Many alternatively spliced transcript variants, some of which are disease-associated mutations, have been described for this gene, but the full-length natures of only some of these variants has been described. A related pseudogene, which is also located on chromosome 17, has been identified. [provided by RefSeq, May 2009].
UOM:  1 * 100 µl
Numéro de catalogue: (BOSSBS-8444R-CY5.5)

Fournisseur:  Bioss
Description:   This gene encodes a nuclear phosphoprotein that plays a role in maintaining genomic stability, and it also acts as a tumor suppressor. The encoded protein combines with other tumor suppressors, DNA damage sensors, and signal transducers to form a large multi-subunit protein complex known as the BRCA1-associated genome surveillance complex (BASC). This gene product associates with RNA polymerase II, and through the C-terminal domain, also interacts with histone deacetylase complexes. This protein thus plays a role in transcription, DNA repair of double-stranded breaks, and recombination. Mutations in this gene are responsible for approximately 40% of inherited breast cancers and more than 80% of inherited breast and ovarian cancers. Alternative splicing plays a role in modulating the subcellular localization and physiological function of this gene. Many alternatively spliced transcript variants, some of which are disease-associated mutations, have been described for this gene, but the full-length natures of only some of these variants has been described. A related pseudogene, which is also located on chromosome 17, has been identified. [provided by RefSeq, May 2009].
UOM:  1 * 100 µl
Numéro de catalogue: (REST20197)

Fournisseur:  Restek
Description:   Set the column flow rate by injection the methane and optimising linear velocity is preferred method for establishing reproducible retention times.
UOM:  1 * 1 ST
Numéro de catalogue: (96030.340)

Fournisseur:  M & I MATERIALS LTD
Description:   This is the softest wax (designed to flow at temperatures of 40-50°C) and suitable for situations where the sealing medium is required to flow into or around a joint.
UOM:  1 * 250 g
Numéro de catalogue: (BOSSBS-5221R-CY7)

Fournisseur:  Bioss
Description:   This gene encodes a nuclear phosphoprotein that plays a role in maintaining genomic stability, and it also acts as a tumor suppressor. The encoded protein combines with other tumor suppressors, DNA damage sensors, and signal transducers to form a large multi-subunit protein complex known as the BRCA1-associated genome surveillance complex (BASC). This gene product associates with RNA polymerase II, and through the C-terminal domain, also interacts with histone deacetylase complexes. This protein thus plays a role in transcription, DNA repair of double-stranded breaks, and recombination. Mutations in this gene are responsible for approximately 40% of inherited breast cancers and more than 80% of inherited breast and ovarian cancers. Alternative splicing plays a role in modulating the subcellular localization and physiological function of this gene. Many alternatively spliced transcript variants, some of which are disease-associated mutations, have been described for this gene, but the full-length natures of only some of these variants has been described. A related pseudogene, which is also located on chromosome 17, has been identified. [provided by RefSeq, May 2009].
UOM:  1 * 100 µl
Numéro de catalogue: (PRSI92-076)

Fournisseur:  ProSci Inc.
Description:   Syntaxin-6 (STX6) is a single-pass type IV membrane protein, which belongs to the Syntaxin family. STX6 is mainly localized in the plasma membrane. STX6 contains one t-SNARE coiled-coil homology domain and involved in intracellular vesicle trafficking. When STX6 function is inhibited, internalization through caveolae is dramaticaliy reduced, whereas other endocytic mechanisms are unaffected. It is reported that STX6 is necessary for proper expression of focal adhesion kinase and integrin alpha5 adhesion receptor.
UOM:  1 * 50 µG
Fournisseur:  Biotium
Description:   NucSpot® Far-Red was designed to be an improved alternative to 7-AAD showing less bleed-through fluorescence in the PE-Texas Red® channel. Ideal for selective detection of dead cells by flow cytometry.
Fournisseur:  Sampling Systems
Description:   The fluid point sampler is designed for taking rapid samples of free-flowing liquids.
Numéro de catalogue: (PRSI5511)

Fournisseur:  ProSci Inc.
Description:   CCDC47 Antibody: The coiled-coil domain is a common protein motif that is often involved in protein oligomerization and is found in proteins such as transcription factors and intermediate filaments. The CCDC47 gene maps to chromosome 17 at 17q23.3. Little is known about this single-pass membrane protein except that the coiled-coil domain is within the cytosolic domain near the carboxy terminus.
UOM:  1 * 1 EA
Fournisseur:  VITLAB
Description:   These starter sets includes three variable VITLAB® micropipettes with different volumes and associated, colour-coded tip boxes and three rack mounts for appropriate storage of micropipettes.
Numéro de catalogue: (LBCP5360630)

Fournisseur:  LABCONCO
Description:   Nexus Horizontal Clean Benches are designed to protect non-hazardous applications, and meet the rigorous demands of life sciences, materials science applications, pharmaceutical R&D and compounding pharmacies. The Nexus also provides an ISO Class 4 clean airflow environment for protection of critical, non-hazardous samples.
UOM:  1 * 1 ST
New Product
Fournisseur:  VWR Collection
Description:   Ce système d’eau de laboratoire compact et prêt à l’emploi constitue le choix idéal pour les utilisateurs qui ont besoin d’une quantité d’eau ultrapure de type I ou d’eau OI (type III) allant jusqu’à 20 litres par jour.
La qualité de l’eau ultrapure fournie satisfait ou excède les exigences des normes ASTM, CLSI, CAP et ISO relatives à l’eau de type I.
Fournisseur:  VWR Collection
Description:   Ce puissant système de purification de l'eau de laboratoire intuitif et puissant procure de l’eau ultrapure supérieure et cohérente de type I et de type II EDI à partir d’eau du robinet. La qualité de l’eau fournie satisfait ou excède les exigences respectives des normes ASTM, CLSI, CAP et ISO relatives à l’eau de type I.

Fournisseur:  Binder
Description:   PT100 temperature sensor - additional flexible PT100, interior, for displaying the temperature on the unit display, Pour: Series FP Avantgarde.Line
UOM:  1 * 1 ST
Numéro de catalogue: (BOSSBS-5221R-A555)

Fournisseur:  Bioss
Description:   This gene encodes a nuclear phosphoprotein that plays a role in maintaining genomic stability, and it also acts as a tumor suppressor. The encoded protein combines with other tumor suppressors, DNA damage sensors, and signal transducers to form a large multi-subunit protein complex known as the BRCA1-associated genome surveillance complex (BASC). This gene product associates with RNA polymerase II, and through the C-terminal domain, also interacts with histone deacetylase complexes. This protein thus plays a role in transcription, DNA repair of double-stranded breaks, and recombination. Mutations in this gene are responsible for approximately 40% of inherited breast cancers and more than 80% of inherited breast and ovarian cancers. Alternative splicing plays a role in modulating the subcellular localization and physiological function of this gene. Many alternatively spliced transcript variants, some of which are disease-associated mutations, have been described for this gene, but the full-length natures of only some of these variants has been described. A related pseudogene, which is also located on chromosome 17, has been identified. [provided by RefSeq, May 2009].
UOM:  1 * 100 µl

Fournisseur:  Bioss
Description:   This gene encodes a nuclear phosphoprotein that plays a role in maintaining genomic stability, and it also acts as a tumor suppressor. The encoded protein combines with other tumor suppressors, DNA damage sensors, and signal transducers to form a large multi-subunit protein complex known as the BRCA1-associated genome surveillance complex (BASC). This gene product associates with RNA polymerase II, and through the C-terminal domain, also interacts with histone deacetylase complexes. This protein thus plays a role in transcription, DNA repair of double-stranded breaks, and recombination. Mutations in this gene are responsible for approximately 40% of inherited breast cancers and more than 80% of inherited breast and ovarian cancers. Alternative splicing plays a role in modulating the subcellular localization and physiological function of this gene. Many alternatively spliced transcript variants, some of which are disease-associated mutations, have been described for this gene, but the full-length natures of only some of these variants has been described. A related pseudogene, which is also located on chromosome 17, has been identified. [provided by RefSeq, May 2009].
UOM:  1 * 100 µl
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