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4,4-Dimethylcyclohexa-1,5-dienylborons\\\\\\\\\\\\\\\\u00E4ure+Mo
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4,4-Dimethylcyclohexa-1,5-dienylborons\\\\\\\\\\\\\\\\u00E4ure+Mo
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Your search request has been modified to limit number of results. Your search was - 4,4-Dimethylcyclohexa-1,5-dienylborons\\\\\\\\\\\\\\\\u00E4ure+Mononatriumsalz |
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Artikel-Nr:
(BOSSBS-1966R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1966R-HRP
Lokale Artikelnummer::
BOSSBS-1966R-HRP
Beschreibung:
May catalyze the degradation of intercellular cohesive structures in the cornified layer of the skin in the continuous shedding of cells from the skin surface. Specific for amino acid residues with aromatic side chains in the P1 position. Cleaves insulin A chain at '14-Tyr-|-Gln-15' and insulin B chain at '6-Leu-|-Cys-7', '16-Tyr-|-Leu-17', '25-Phe-|-Tyr-26' and '26-Tyr-|-Thr-27'. Could play a role in the activation of precursors to inflammatory cytokines.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7921R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7921R-CY3
Lokale Artikelnummer::
BOSSBS-7921R-CY3
Beschreibung:
Receptor for SLIT2, and probably SLIT1, which are thought to act as molecular guidance cue in cellular migration, including axonal navigation at the ventral midline of the neural tube and projection of axons to different regions during neuronal development.Involvement in disease:Defects in ROBO2 are the cause of vesicoureteral reflux type 2 (VUR2) . VUR is a complex, genetically heterogeneous developmental disorder characterized by the retrograde flow of urine from the bladder into the ureter and is associated with reflux nephropathy, the cause of 15% of end-stage renal disease in children and young adults.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7921R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7921R-A647
Lokale Artikelnummer::
BOSSBS-7921R-A647
Beschreibung:
Receptor for SLIT2, and probably SLIT1, which are thought to act as molecular guidance cue in cellular migration, including axonal navigation at the ventral midline of the neural tube and projection of axons to different regions during neuronal development.Involvement in disease:Defects in ROBO2 are the cause of vesicoureteral reflux type 2 (VUR2) . VUR is a complex, genetically heterogeneous developmental disorder characterized by the retrograde flow of urine from the bladder into the ureter and is associated with reflux nephropathy, the cause of 15% of end-stage renal disease in children and young adults.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15460R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15460R-FITC
Lokale Artikelnummer::
BOSSBS-15460R-FITC
Beschreibung:
HERC2 is a belongs to the HERC gene family that encodes a group of unusually large proteins, which contain multiple structural domains. All members have at least 1 copy of an N-terminal region showing homology to the cell cycle regulator RCC1 and a C-terminal HECT (homologous to E6-AP C terminus) domain found in a number of E3 ubiquitin protein ligases. Genetic variations in this gene are associated with skin/hair/eye pigmentation variability. Multiple pseudogenes of this gene are located on chromosomes 15 and 16.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15460R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15460R-HRP
Lokale Artikelnummer::
BOSSBS-15460R-HRP
Beschreibung:
HERC2 is a belongs to the HERC gene family that encodes a group of unusually large proteins, which contain multiple structural domains. All members have at least 1 copy of an N-terminal region showing homology to the cell cycle regulator RCC1 and a C-terminal HECT (homologous to E6-AP C terminus) domain found in a number of E3 ubiquitin protein ligases. Genetic variations in this gene are associated with skin/hair/eye pigmentation variability. Multiple pseudogenes of this gene are located on chromosomes 15 and 16.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7921R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7921R-A680
Lokale Artikelnummer::
BOSSBS-7921R-A680
Beschreibung:
Receptor for SLIT2, and probably SLIT1, which are thought to act as molecular guidance cue in cellular migration, including axonal navigation at the ventral midline of the neural tube and projection of axons to different regions during neuronal development.Involvement in disease:Defects in ROBO2 are the cause of vesicoureteral reflux type 2 (VUR2) . VUR is a complex, genetically heterogeneous developmental disorder characterised by the retrograde flow of urine from the bladder into the ureter and is associated with reflux nephropathy, the cause of 15% of end-stage renal disease in children and young adults.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15460R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15460R-A647
Lokale Artikelnummer::
BOSSBS-15460R-A647
Beschreibung:
HERC2 is a belongs to the HERC gene family that encodes a group of unusually large proteins, which contain multiple structural domains. All members have at least 1 copy of an N-terminal region showing homology to the cell cycle regulator RCC1 and a C-terminal HECT (homologous to E6-AP C terminus) domain found in a number of E3 ubiquitin protein ligases. Genetic variations in this gene are associated with skin/hair/eye pigmentation variability. Multiple pseudogenes of this gene are located on chromosomes 15 and 16.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15460R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15460R-A555
Lokale Artikelnummer::
BOSSBS-15460R-A555
Beschreibung:
HERC2 is a belongs to the HERC gene family that encodes a group of unusually large proteins, which contain multiple structural domains. All members have at least 1 copy of an N-terminal region showing homology to the cell cycle regulator RCC1 and a C-terminal HECT (homologous to E6-AP C terminus) domain found in a number of E3 ubiquitin protein ligases. Genetic variations in this gene are associated with skin/hair/eye pigmentation variability. Multiple pseudogenes of this gene are located on chromosomes 15 and 16.
VE:
1 * 100 µl
Artikel-Nr:
(FRIT18.3020.00)
Lieferant:
FRITSCH
Hersteller-Artikelnummer::
18.3020.00
Lokale Artikelnummer::
FRIT18.3020.00
Beschreibung:
The Analysette®18 heavy duty analytical sieve shaker was specially designed for large sieving quantities. It can effortlessly sieve up to 15 kg of material between 20 μm and 125 mm. This sieving unit is particularly suitable for particle size analysis and portioning of coarse-grained materials through dry sieving or wet sieving with conversion kit.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-7921R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7921R-CY7
Lokale Artikelnummer::
BOSSBS-7921R-CY7
Beschreibung:
Receptor for SLIT2, and probably SLIT1, which are thought to act as molecular guidance cue in cellular migration, including axonal navigation at the ventral midline of the neural tube and projection of axons to different regions during neuronal development.Involvement in disease:Defects in ROBO2 are the cause of vesicoureteral reflux type 2 (VUR2) . VUR is a complex, genetically heterogeneous developmental disorder characterized by the retrograde flow of urine from the bladder into the ureter and is associated with reflux nephropathy, the cause of 15% of end-stage renal disease in children and young adults.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7921R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7921R-A750
Lokale Artikelnummer::
BOSSBS-7921R-A750
Beschreibung:
Receptor for SLIT2, and probably SLIT1, which are thought to act as molecular guidance cue in cellular migration, including axonal navigation at the ventral midline of the neural tube and projection of axons to different regions during neuronal development.Involvement in disease:Defects in ROBO2 are the cause of vesicoureteral reflux type 2 (VUR2) . VUR is a complex, genetically heterogeneous developmental disorder characterised by the retrograde flow of urine from the bladder into the ureter and is associated with reflux nephropathy, the cause of 15% of end-stage renal disease in children and young adults.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7921R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7921R-A555
Lokale Artikelnummer::
BOSSBS-7921R-A555
Beschreibung:
Receptor for SLIT2, and probably SLIT1, which are thought to act as molecular guidance cue in cellular migration, including axonal navigation at the ventral midline of the neural tube and projection of axons to different regions during neuronal development.Involvement in disease:Defects in ROBO2 are the cause of vesicoureteral reflux type 2 (VUR2) . VUR is a complex, genetically heterogeneous developmental disorder characterized by the retrograde flow of urine from the bladder into the ureter and is associated with reflux nephropathy, the cause of 15% of end-stage renal disease in children and young adults.
VE:
1 * 100 µl
Lieferant:
Biotium
Beschreibung:
The mouse monoclonal antibody recognizes CD1b, a 44 kDa type I glycoprotein associated with beta2-microglobulin. It is expressed on dendritic cells, Langerhans cells, thymocytes, and T acute lymphoblastic leukemia cells. The CD1 multigene family encodes five forms of the CD1 T-cell surface glycoprotein in human, designated CD1A, 1B, 1C, 1D and 1E. CD1, a type 1 membrane protein, has structural similarity to the MHC class I antigen and has been shown to present lipid antigens for recognition by T lymphocytes. Constitutive endocytosis of CD1B molecules and the differential sorting of MHC class II from lysosomes separate peptide- and lipid antigen-presenting molecules during dendritic cell maturation. CD1B is also expressed in interdigitating cells.
Lieferant:
Biotium
Beschreibung:
The mouse monoclonal antibody recognizes CD1b, a 44 kDa type I glycoprotein associated with beta2-microglobulin. It is expressed on dendritic cells, Langerhans cells, thymocytes, and T acute lymphoblastic leukemia cells. The CD1 multigene family encodes five forms of the CD1 T-cell surface glycoprotein in human, designated CD1A, 1B, 1C, 1D and 1E. CD1, a type 1 membrane protein, has structural similarity to the MHC class I antigen and has been shown to present lipid antigens for recognition by T lymphocytes. Constitutive endocytosis of CD1B molecules and the differential sorting of MHC class II from lysosomes separate peptide- and lipid antigen-presenting molecules during dendritic cell maturation. CD1B is also expressed in interdigitating cells.
Lieferant:
Biotium
Beschreibung:
The mouse monoclonal antibody recognizes CD1b, a 44 kDa type I glycoprotein associated with beta2-microglobulin. It is expressed on dendritic cells, Langerhans cells, thymocytes, and T acute lymphoblastic leukemia cells. The CD1 multigene family encodes five forms of the CD1 T-cell surface glycoprotein in human, designated CD1A, 1B, 1C, 1D and 1E. CD1, a type 1 membrane protein, has structural similarity to the MHC class I antigen and has been shown to present lipid antigens for recognition by T lymphocytes. Constitutive endocytosis of CD1B molecules and the differential sorting of MHC class II from lysosomes separate peptide- and lipid antigen-presenting molecules during dendritic cell maturation. CD1B is also expressed in interdigitating cells.
Artikel-Nr:
(PRSI33-075)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
33-075
Lokale Artikelnummer::
PRSI33-075
Beschreibung:
This antibody recognises a protein of 55 to 62 kDa, identified as Cyclin B1. In mammals, Cyclin B1 associates with inactive p34cdc2, which facilitates phosphorylation of p34cdc2 at amino acids Thr-14 and Tyr-15. This maintains the inactive state until the end of G2-phase. The inactive Cyclin B1-p34cdc2 complex continues to accumulate in the cytoplasm until the completion of DNA synthesis, when Cdc25, a specific protein phosphatase, dephosphorylates amino acids Thr-14 and Tyr-15 of p34cdc2 rendering the complex active at the G2/M boundary. This mitotic kinase complex remains active until the metaphase/anaphase transition when Cyclin B1 is degraded. This degradation process is ubiquitin-dependent and is necessary for the cell to exit mitosis. Cyclin B1-p34cdc2 plays a critical role in G2 to M transition.
VE:
1 * 100 µG
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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