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460 results for "CPC+COLDER"

460 Results for: "CPC+COLDER"

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CPC® Quick-Disconnect Fittings, Compression Inserts

CPC® Quick-Disconnect Fittings, Compression Inserts

Supplier: Avantor Fluid Handling

No more struggling - just press thumb latch.

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Anti-c-phycocyanin Rabbit Polyclonal Antibody (Cy7®)

Supplier: Bioss

C-Phycocyanin (CPC), a pigment-protein complex from the light-harvesting phycobiliprotein family.

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Anti-CDCA8 Rabbit Polyclonal Antibody (Cy7®)

Supplier: Bioss

Component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chromatin-induced microtubule stabilization and spindle assembly. In the complex, it may be required to direct the CPC to centromeric DNA. Major effector of the TTK kinase in the control of attachment-error-correction and chromosome alignment.

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Anti-CDCA8 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Supplier: Bioss

Component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chromatin-induced microtubule stabilization and spindle assembly. In the complex, it may be required to direct the CPC to centromeric DNA. Major effector of the TTK kinase in the control of attachment-error-correction and chromosome alignment.

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Anti-c-phycocyanin Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Supplier: Bioss

C-Phycocyanin (CPC), a pigment-protein complex from the light-harvesting phycobiliprotein family.

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Anti-c-phycocyanin Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Supplier: Bioss

C-Phycocyanin (CPC), a pigment-protein complex from the light-harvesting phycobiliprotein family.

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CPC® High-Flow Plastic Quick-Disconnect Fittings, Hose Barb Inserts

CPC® High-Flow Plastic Quick-Disconnect Fittings, Hose Barb Inserts

Supplier: Avantor Fluid Handling

Fittings connect in a snap.

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CPC® High-Flow Quick-Disconnect Fittings, Threaded Bodies

CPC® High-Flow Quick-Disconnect Fittings, Threaded Bodies

Supplier: Avantor Fluid Handling

No more leaks - valved couplings automatically shut off flow.

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CPC® Plastic Quick-Disconnect Fittings, NPT Threaded Bodies

CPC® Plastic Quick-Disconnect Fittings, NPT Threaded Bodies

Supplier: Avantor Fluid Handling

Fittings connect in a snap.

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Anti-c-phycocyanin Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Supplier: Bioss

C-Phycocyanin (CPC), a pigment-protein complex from the light-harvesting phycobiliprotein family.

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Anti-c-phycocyanin Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Supplier: Bioss

C-Phycocyanin (CPC), a pigment-protein complex from the light-harvesting phycobiliprotein family.

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CPC® Quick-Disconnect Fittings, Compression Elbow Inserts

CPC® Quick-Disconnect Fittings, Compression Elbow Inserts

Supplier: Avantor Fluid Handling

No more struggling - just press thumb latch.

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CPC® Plastic Quick-Disconnect Fittings, Hose Barb Inserts

CPC® Plastic Quick-Disconnect Fittings, Hose Barb Inserts

Supplier: Avantor Fluid Handling

Fittings connect in a snap.

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Anti-AURKB Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Supplier: Bioss

Serine/threonine-protein kinase component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chromatin-induced microtubule stabilization and spindle assembly. Involved in the bipolar attachment of spindle microtubules to kinetochores and is a key regulator for the onset of cytokinesis during mitosis. Required for central/midzone spindle assembly and cleavage furrow formation. Key component of the cytokinesis checkpoint, a process required to delay abscission to prevent both premature resolution of intercellular chromosome bridges and accumulation of DNA damage: phosphorylates CHMP4C, leading to retain abscission-competent VPS4 (VPS4A and/or VPS4B) at the midbody ring until abscission checkpoint signaling is terminated at late cytokinesis (PubMed:22422861, PubMed:24814515). AURKB phosphorylates the CPC complex subunits BIRC5/survivin, CDCA8/borealin and INCENP. Phosphorylation of INCENP leads to increased AURKB activity. Other known AURKB substrates involved in centromeric functions and mitosis are CENPA, DES/desmin, GPAF, KIF2C, NSUN2, RACGAP1, SEPT1, VIM/vimentin, GSG2/Haspin, and histone H3. A positive feedback loop involving GSG2 and AURKB contributes to localization of CPC to centromeres. Phosphorylation of VIM controls vimentin filament segregation in cytokinetic process, whereas histone H3 is phosphorylated at 'Ser-10' and 'Ser-28' during mitosis (H3S10ph and H3S28ph, respectively). A positive feedback between GSG2 and AURKB contributes to CPC localization. AURKB is also required for kinetochore localization of BUB1 and SGOL1. Phosphorylation of p53/TP53 negatively regulates its transcriptional activity. Key regulator of active promoters in resting B- and T-lymphocytes.

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Anti-AURKB Rabbit Polyclonal Antibody (Cy5.5®)

Supplier: Bioss

Serine/threonine-protein kinase component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chromatin-induced microtubule stabilization and spindle assembly. Involved in the bipolar attachment of spindle microtubules to kinetochores and is a key regulator for the onset of cytokinesis during mitosis. Required for central/midzone spindle assembly and cleavage furrow formation. Key component of the cytokinesis checkpoint, a process required to delay abscission to prevent both premature resolution of intercellular chromosome bridges and accumulation of DNA damage: phosphorylates CHMP4C, leading to retain abscission-competent VPS4 (VPS4A and/or VPS4B) at the midbody ring until abscission checkpoint signaling is terminated at late cytokinesis (PubMed:22422861, PubMed:24814515). AURKB phosphorylates the CPC complex subunits BIRC5/survivin, CDCA8/borealin and INCENP. Phosphorylation of INCENP leads to increased AURKB activity. Other known AURKB substrates involved in centromeric functions and mitosis are CENPA, DES/desmin, GPAF, KIF2C, NSUN2, RACGAP1, SEPT1, VIM/vimentin, GSG2/Haspin, and histone H3. A positive feedback loop involving GSG2 and AURKB contributes to localization of CPC to centromeres. Phosphorylation of VIM controls vimentin filament segregation in cytokinetic process, whereas histone H3 is phosphorylated at 'Ser-10' and 'Ser-28' during mitosis (H3S10ph and H3S28ph, respectively). A positive feedback between GSG2 and AURKB contributes to CPC localization. AURKB is also required for kinetochore localization of BUB1 and SGOL1. Phosphorylation of p53/TP53 negatively regulates its transcriptional activity. Key regulator of active promoters in resting B- and T-lymphocytes.

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Anti-c-phycocyanin Rabbit Polyclonal Antibody

Supplier: Bioss

C-Phycocyanin (CPC), a pigment-protein complex from the light-harvesting phycobiliprotein family.

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CPC® Miniature Quick-Disconnect Fittings, Hose Barb Inserts

CPC® Miniature Quick-Disconnect Fittings, Hose Barb Inserts

Supplier: Avantor Fluid Handling

No more kinked tubing - allows tubing to rotate freely.

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CPC® Quick-Disconnect Fittings, Hose Barb Elbow Inserts

CPC® Quick-Disconnect Fittings, Hose Barb Elbow Inserts

Supplier: Avantor Fluid Handling

No more struggling - just press thumb latch.

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Anti-AURKB Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Supplier: Bioss

Serine/threonine-protein kinase component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chromatin-induced microtubule stabilization and spindle assembly. Involved in the bipolar attachment of spindle microtubules to kinetochores and is a key regulator for the onset of cytokinesis during mitosis. Required for central/midzone spindle assembly and cleavage furrow formation. Key component of the cytokinesis checkpoint, a process required to delay abscission to prevent both premature resolution of intercellular chromosome bridges and accumulation of DNA damage: phosphorylates CHMP4C, leading to retain abscission-competent VPS4 (VPS4A and/or VPS4B) at the midbody ring until abscission checkpoint signaling is terminated at late cytokinesis (PubMed:22422861, PubMed:24814515). AURKB phosphorylates the CPC complex subunits BIRC5/survivin, CDCA8/borealin and INCENP. Phosphorylation of INCENP leads to increased AURKB activity. Other known AURKB substrates involved in centromeric functions and mitosis are CENPA, DES/desmin, GPAF, KIF2C, NSUN2, RACGAP1, SEPT1, VIM/vimentin, GSG2/Haspin, and histone H3. A positive feedback loop involving GSG2 and AURKB contributes to localization of CPC to centromeres. Phosphorylation of VIM controls vimentin filament segregation in cytokinetic process, whereas histone H3 is phosphorylated at 'Ser-10' and 'Ser-28' during mitosis (H3S10ph and H3S28ph, respectively). A positive feedback between GSG2 and AURKB contributes to CPC localization. AURKB is also required for kinetochore localization of BUB1 and SGOL1. Phosphorylation of p53/TP53 negatively regulates its transcriptional activity. Key regulator of active promoters in resting B- and T-lymphocytes.

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Anti-AURKB Rabbit Polyclonal Antibody (Cy7®)

Supplier: Bioss

Serine/threonine-protein kinase component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chromatin-induced microtubule stabilization and spindle assembly. Involved in the bipolar attachment of spindle microtubules to kinetochores and is a key regulator for the onset of cytokinesis during mitosis. Required for central/midzone spindle assembly and cleavage furrow formation. Key component of the cytokinesis checkpoint, a process required to delay abscission to prevent both premature resolution of intercellular chromosome bridges and accumulation of DNA damage: phosphorylates CHMP4C, leading to retain abscission-competent VPS4 (VPS4A and/or VPS4B) at the midbody ring until abscission checkpoint signaling is terminated at late cytokinesis (PubMed:22422861, PubMed:24814515). AURKB phosphorylates the CPC complex subunits BIRC5/survivin, CDCA8/borealin and INCENP. Phosphorylation of INCENP leads to increased AURKB activity. Other known AURKB substrates involved in centromeric functions and mitosis are CENPA, DES/desmin, GPAF, KIF2C, NSUN2, RACGAP1, SEPT1, VIM/vimentin, GSG2/Haspin, and histone H3. A positive feedback loop involving GSG2 and AURKB contributes to localization of CPC to centromeres. Phosphorylation of VIM controls vimentin filament segregation in cytokinetic process, whereas histone H3 is phosphorylated at 'Ser-10' and 'Ser-28' during mitosis (H3S10ph and H3S28ph, respectively). A positive feedback between GSG2 and AURKB contributes to CPC localization. AURKB is also required for kinetochore localization of BUB1 and SGOL1. Phosphorylation of p53/TP53 negatively regulates its transcriptional activity. Key regulator of active promoters in resting B- and T-lymphocytes.

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Anti-c-phycocyanin Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Supplier: Bioss

C-Phycocyanin (CPC), a pigment-protein complex from the light-harvesting phycobiliprotein family.

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Anti-c-phycocyanin Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Supplier: Bioss

C-Phycocyanin (CPC), a pigment-protein complex from the light-harvesting phycobiliprotein family.

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CPC® Metal Quick-Disconnect Fittings, Panel-Mount Compression Body

CPC® Metal Quick-Disconnect Fittings, Panel-Mount Compression Body

Supplier: Avantor Fluid Handling

Convenience of a quick-disconnect in pressure and vacuum applications.

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CPC® Metal Quick-Disconnect Fittings, Panel-Mount Hose Barb Inert

CPC® Metal Quick-Disconnect Fittings, Panel-Mount Hose Barb Inert

Supplier: Avantor Fluid Handling

Convenience of a quick-disconnect in pressure and vacuum applications.

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CPC® High-Flow Quick-Disconnect Fittings, Hose Barb Inserts

CPC® High-Flow Quick-Disconnect Fittings, Hose Barb Inserts

Supplier: Avantor Fluid Handling

No more leaks - valved couplings automatically shut off flow.

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CPC® High-Flow Quick-Disconnect Fittings, Hose Barb Bodies

CPC® High-Flow Quick-Disconnect Fittings, Hose Barb Bodies

Supplier: Avantor Fluid Handling

No more leaks - valved couplings automatically shut off flow.

Expand 22 Items
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CPC® Metal Quick-Disconnect Fittings, Compression Inserts

CPC® Metal Quick-Disconnect Fittings, Compression Inserts

Supplier: Avantor Fluid Handling

Convenience of a quick-disconnect in pressure and vacuum applications.

Expand 9 Items
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Anti-AURKB Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Supplier: Bioss

Serine/threonine-protein kinase component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chromatin-induced microtubule stabilization and spindle assembly. Involved in the bipolar attachment of spindle microtubules to kinetochores and is a key regulator for the onset of cytokinesis during mitosis. Required for central/midzone spindle assembly and cleavage furrow formation. Key component of the cytokinesis checkpoint, a process required to delay abscission to prevent both premature resolution of intercellular chromosome bridges and accumulation of DNA damage: phosphorylates CHMP4C, leading to retain abscission-competent VPS4 (VPS4A and/or VPS4B) at the midbody ring until abscission checkpoint signaling is terminated at late cytokinesis (PubMed:22422861, PubMed:24814515). AURKB phosphorylates the CPC complex subunits BIRC5/survivin, CDCA8/borealin and INCENP. Phosphorylation of INCENP leads to increased AURKB activity. Other known AURKB substrates involved in centromeric functions and mitosis are CENPA, DES/desmin, GPAF, KIF2C, NSUN2, RACGAP1, SEPT1, VIM/vimentin, GSG2/Haspin, and histone H3. A positive feedback loop involving GSG2 and AURKB contributes to localization of CPC to centromeres. Phosphorylation of VIM controls vimentin filament segregation in cytokinetic process, whereas histone H3 is phosphorylated at 'Ser-10' and 'Ser-28' during mitosis (H3S10ph and H3S28ph, respectively). A positive feedback between GSG2 and AURKB contributes to CPC localization. AURKB is also required for kinetochore localization of BUB1 and SGOL1. Phosphorylation of p53/TP53 negatively regulates its transcriptional activity. Key regulator of active promoters in resting B- and T-lymphocytes.

Expand 1 Items
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Anti-AURKB Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Supplier: Bioss

Serine/threonine-protein kinase component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chromatin-induced microtubule stabilization and spindle assembly. Involved in the bipolar attachment of spindle microtubules to kinetochores and is a key regulator for the onset of cytokinesis during mitosis. Required for central/midzone spindle assembly and cleavage furrow formation. Key component of the cytokinesis checkpoint, a process required to delay abscission to prevent both premature resolution of intercellular chromosome bridges and accumulation of DNA damage: phosphorylates CHMP4C, leading to retain abscission-competent VPS4 (VPS4A and/or VPS4B) at the midbody ring until abscission checkpoint signaling is terminated at late cytokinesis (PubMed:22422861, PubMed:24814515). AURKB phosphorylates the CPC complex subunits BIRC5/survivin, CDCA8/borealin and INCENP. Phosphorylation of INCENP leads to increased AURKB activity. Other known AURKB substrates involved in centromeric functions and mitosis are CENPA, DES/desmin, GPAF, KIF2C, NSUN2, RACGAP1, SEPT1, VIM/vimentin, GSG2/Haspin, and histone H3. A positive feedback loop involving GSG2 and AURKB contributes to localization of CPC to centromeres. Phosphorylation of VIM controls vimentin filament segregation in cytokinetic process, whereas histone H3 is phosphorylated at 'Ser-10' and 'Ser-28' during mitosis (H3S10ph and H3S28ph, respectively). A positive feedback between GSG2 and AURKB contributes to CPC localization. AURKB is also required for kinetochore localization of BUB1 and SGOL1. Phosphorylation of p53/TP53 negatively regulates its transcriptional activity. Key regulator of active promoters in resting B- and T-lymphocytes.

Expand 1 Items
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Anti-AURKB Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Supplier: Bioss

Serine/threonine-protein kinase component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chromatin-induced microtubule stabilization and spindle assembly. Involved in the bipolar attachment of spindle microtubules to kinetochores and is a key regulator for the onset of cytokinesis during mitosis. Required for central/midzone spindle assembly and cleavage furrow formation. Key component of the cytokinesis checkpoint, a process required to delay abscission to prevent both premature resolution of intercellular chromosome bridges and accumulation of DNA damage: phosphorylates CHMP4C, leading to retain abscission-competent VPS4 (VPS4A and/or VPS4B) at the midbody ring until abscission checkpoint signaling is terminated at late cytokinesis (PubMed:22422861, PubMed:24814515). AURKB phosphorylates the CPC complex subunits BIRC5/survivin, CDCA8/borealin and INCENP. Phosphorylation of INCENP leads to increased AURKB activity. Other known AURKB substrates involved in centromeric functions and mitosis are CENPA, DES/desmin, GPAF, KIF2C, NSUN2, RACGAP1, SEPT1, VIM/vimentin, GSG2/Haspin, and histone H3. A positive feedback loop involving GSG2 and AURKB contributes to localization of CPC to centromeres. Phosphorylation of VIM controls vimentin filament segregation in cytokinetic process, whereas histone H3 is phosphorylated at 'Ser-10' and 'Ser-28' during mitosis (H3S10ph and H3S28ph, respectively). A positive feedback between GSG2 and AURKB contributes to CPC localization. AURKB is also required for kinetochore localization of BUB1 and SGOL1. Phosphorylation of p53/TP53 negatively regulates its transcriptional activity. Key regulator of active promoters in resting B- and T-lymphocytes.

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