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Codice catalogo: (BOSSBS-11742R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-11742R-CY3
Codice articolo locale: BOSSBS-11742R-CY3
Descrizione: Myotonic dystrophy protein kinase is a multi-domain protein kinase found in muscle that is activated in response to G protein second messengers and proteolysis (1). DMPK is implicated in myotonic muscular dystrophy (DM), an autosomal dominant-inherited disorder that predominately affects skeletal and cardiac muscle and causes defects in cardiac conduction (2,3). DM arises through expansion of CTG repeats in the 3’-UTR of the DMPK gene (4). Mutant DMPK transcripts with an extended region of CUG repeats are retained in the nucleus (5). These transcripts also influence the expression of the DM locus-associated homeodomain protein (DMAHP)/SIX5, to mediate in part the DM phenotype (6). Other substrates for DMPK include myogenin, L-type calcium channels, and Phospholemman (PLM) (1).
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11742R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-11742R-CY7
Codice articolo locale: BOSSBS-11742R-CY7
Descrizione: Myotonic dystrophy protein kinase is a multi-domain protein kinase found in muscle that is activated in response to G protein second messengers and proteolysis (1). DMPK is implicated in myotonic muscular dystrophy (DM), an autosomal dominant-inherited disorder that predominately affects skeletal and cardiac muscle and causes defects in cardiac conduction (2,3). DM arises through expansion of CTG repeats in the 3’-UTR of the DMPK gene (4). Mutant DMPK transcripts with an extended region of CUG repeats are retained in the nucleus (5). These transcripts also influence the expression of the DM locus-associated homeodomain protein (DMAHP)/SIX5, to mediate in part the DM phenotype (6). Other substrates for DMPK include myogenin, L-type calcium channels, and Phospholemman (PLM) (1).
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11742R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-11742R-CY5
Codice articolo locale: BOSSBS-11742R-CY5
Descrizione: Myotonic dystrophy protein kinase is a multi-domain protein kinase found in muscle that is activated in response to G protein second messengers and proteolysis (1). DMPK is implicated in myotonic muscular dystrophy (DM), an autosomal dominant-inherited disorder that predominately affects skeletal and cardiac muscle and causes defects in cardiac conduction (2,3). DM arises through expansion of CTG repeats in the 3’-UTR of the DMPK gene (4). Mutant DMPK transcripts with an extended region of CUG repeats are retained in the nucleus (5). These transcripts also influence the expression of the DM locus-associated homeodomain protein (DMAHP)/SIX5, to mediate in part the DM phenotype (6). Other substrates for DMPK include myogenin, L-type calcium channels, and Phospholemman (PLM) (1).
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11742R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-11742R-A488
Codice articolo locale: BOSSBS-11742R-A488
Descrizione: Myotonic dystrophy protein kinase is a multi-domain protein kinase found in muscle that is activated in response to G protein second messengers and proteolysis (1). DMPK is implicated in myotonic muscular dystrophy (DM), an autosomal dominant-inherited disorder that predominately affects skeletal and cardiac muscle and causes defects in cardiac conduction (2,3). DM arises through expansion of CTG repeats in the 3’-UTR of the DMPK gene (4). Mutant DMPK transcripts with an extended region of CUG repeats are retained in the nucleus (5). These transcripts also influence the expression of the DM locus-associated homeodomain protein (DMAHP)/SIX5, to mediate in part the DM phenotype (6). Other substrates for DMPK include myogenin, L-type calcium channels, and Phospholemman (PLM) (1).
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11742R)
Fornitore: Bioss
Codice articolo fornitore: BS-11742R
Codice articolo locale: BOSSBS-11742R
Descrizione: Myotonic dystrophy protein kinase is a multi-domain protein kinase found in muscle that is activated in response to G protein second messengers and proteolysis (1). DMPK is implicated in myotonic muscular dystrophy (DM), an autosomal dominant-inherited disorder that predominately affects skeletal and cardiac muscle and causes defects in cardiac conduction (2,3). DM arises through expansion of CTG repeats in the 3’-UTR of the DMPK gene (4). Mutant DMPK transcripts with an extended region of CUG repeats are retained in the nucleus (5). These transcripts also influence the expression of the DM locus-associated homeodomain protein (DMAHP)/SIX5, to mediate in part the DM phenotype (6). Other substrates for DMPK include myogenin, L-type calcium channels, and Phospholemman (PLM) (1).
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11742R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-11742R-A647
Codice articolo locale: BOSSBS-11742R-A647
Descrizione: Myotonic dystrophy protein kinase is a multi-domain protein kinase found in muscle that is activated in response to G protein second messengers and proteolysis (1). DMPK is implicated in myotonic muscular dystrophy (DM), an autosomal dominant-inherited disorder that predominately affects skeletal and cardiac muscle and causes defects in cardiac conduction (2,3). DM arises through expansion of CTG repeats in the 3’-UTR of the DMPK gene (4). Mutant DMPK transcripts with an extended region of CUG repeats are retained in the nucleus (5). These transcripts also influence the expression of the DM locus-associated homeodomain protein (DMAHP)/SIX5, to mediate in part the DM phenotype (6). Other substrates for DMPK include myogenin, L-type calcium channels, and Phospholemman (PLM) (1).
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11742R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-11742R-A555
Codice articolo locale: BOSSBS-11742R-A555
Descrizione: Myotonic dystrophy protein kinase is a multi-domain protein kinase found in muscle that is activated in response to G protein second messengers and proteolysis (1). DMPK is implicated in myotonic muscular dystrophy (DM), an autosomal dominant-inherited disorder that predominately affects skeletal and cardiac muscle and causes defects in cardiac conduction (2,3). DM arises through expansion of CTG repeats in the 3’-UTR of the DMPK gene (4). Mutant DMPK transcripts with an extended region of CUG repeats are retained in the nucleus (5). These transcripts also influence the expression of the DM locus-associated homeodomain protein (DMAHP)/SIX5, to mediate in part the DM phenotype (6). Other substrates for DMPK include myogenin, L-type calcium channels, and Phospholemman (PLM) (1).
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11742R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-11742R-HRP
Codice articolo locale: BOSSBS-11742R-HRP
Descrizione: Myotonic dystrophy protein kinase is a multi-domain protein kinase found in muscle that is activated in response to G protein second messengers and proteolysis (1). DMPK is implicated in myotonic muscular dystrophy (DM), an autosomal dominant-inherited disorder that predominately affects skeletal and cardiac muscle and causes defects in cardiac conduction (2,3). DM arises through expansion of CTG repeats in the 3’-UTR of the DMPK gene (4). Mutant DMPK transcripts with an extended region of CUG repeats are retained in the nucleus (5). These transcripts also influence the expression of the DM locus-associated homeodomain protein (DMAHP)/SIX5, to mediate in part the DM phenotype (6). Other substrates for DMPK include myogenin, L-type calcium channels, and Phospholemman (PLM) (1).
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11742R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-11742R-A350
Codice articolo locale: BOSSBS-11742R-A350
Descrizione: Myotonic dystrophy protein kinase is a multi-domain protein kinase found in muscle that is activated in response to G protein second messengers and proteolysis (1). DMPK is implicated in myotonic muscular dystrophy (DM), an autosomal dominant-inherited disorder that predominately affects skeletal and cardiac muscle and causes defects in cardiac conduction (2,3). DM arises through expansion of CTG repeats in the 3’-UTR of the DMPK gene (4). Mutant DMPK transcripts with an extended region of CUG repeats are retained in the nucleus (5). These transcripts also influence the expression of the DM locus-associated homeodomain protein (DMAHP)/SIX5, to mediate in part the DM phenotype (6). Other substrates for DMPK include myogenin, L-type calcium channels, and Phospholemman (PLM) (1).
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11742R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-11742R-FITC
Codice articolo locale: BOSSBS-11742R-FITC
Descrizione: Myotonic dystrophy protein kinase is a multi-domain protein kinase found in muscle that is activated in response to G protein second messengers and proteolysis (1). DMPK is implicated in myotonic muscular dystrophy (DM), an autosomal dominant-inherited disorder that predominately affects skeletal and cardiac muscle and causes defects in cardiac conduction (2,3). DM arises through expansion of CTG repeats in the 3’-UTR of the DMPK gene (4). Mutant DMPK transcripts with an extended region of CUG repeats are retained in the nucleus (5). These transcripts also influence the expression of the DM locus-associated homeodomain protein (DMAHP)/SIX5, to mediate in part the DM phenotype (6). Other substrates for DMPK include myogenin, L-type calcium channels, and Phospholemman (PLM) (1).
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11742R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-11742R-A750
Codice articolo locale: BOSSBS-11742R-A750
Descrizione: Myotonic dystrophy protein kinase is a multi-domain protein kinase found in muscle that is activated in response to G protein second messengers and proteolysis. DMPK is implicated in myotonic muscular dystrophy (DM), an autosomal dominant-inherited disorder that predominately affects skeletal and cardiac muscle and causes defects in cardiac conduction. DM arises through expansion of CTG repeats in the 3 UTR of the DMPK gene. Mutant DMPK transcripts with an extended region of CUG repeats are retained in the nucleus. These transcripts also influence the expression of the DM locus-associated homeodomain protein (DMAHP)/SIX5, to mediate in part the DM phenotype. Other substrates for DMPK include myogenin, L-type calcium channels, and Phospholemman (PLM).
UOM: 1 * 100 µl


Codice catalogo: (50050.)
Fornitore: Biotium
Codice articolo fornitore: 50050
Codice articolo locale: BTIU50050
Descrizione: DMNP-EDTA (also known as DM-Nitrophen™) is a caged Ca2+ chelator. Upon photolysis, the Kd for Ca2+ increases from 5 nM to 3 mM, resulting in a pulse of free Ca2+.
UOM: 1 * 5 mg


Codice catalogo: (BSBTPA1788)
Fornitore: Boster Bio
Codice articolo fornitore: PA1788
Codice articolo locale: BSBTPA1788
Descrizione: Rabbit IgG polyclonal antibody for HLA class II histocompatibility antigen, DM beta chain (HLA-DMB) detection. Tested with WB, IHC-P in Human.
UOM: 1 * 0,1 mg


Codice catalogo: (PB006C-1-DM2)
Fornitore: Charles River Laboratories Cell Solutions
Codice articolo fornitore: PB006C-1-DM2
Codice articolo locale: HCMSPB006C-1-DM2
Descrizione: Human peripheral blood plasma used for researching the causes, diagnosis, supportive care and treatment of type 2 diabetes mellitus (DM 2). Collected from IRB-consented donors diagnosed with type 2 diabetes mellitus.
UOM: 1 * 2 mL


Codice catalogo: (PRSI27-808)
Fornitore: ProSci Inc.
Codice articolo fornitore: 27-808
Codice articolo locale: PRSI27-808
Descrizione: DMRTA2 is involved in gonadal differentiation. The gene is part of five novel human DM genes that map to three well-defined regions of chromosomes 1, 9, and 19 (one gene on chromosome 19 having an additional homolog on chromosome X).
UOM: 1 * 50 µG


Fornitore: Tonbo Biosciences
Descrizione: The Mouse Dendritic Cell backbone panel is a six-color combination of anti-mouse antibodies. This panel can serve as a backbone for identifying major dendritic cell (DC) subsets (Duriancik DM and Hoag KA. 2009. Cytometry. 75A: 951-959). Hosts: Rat, Armenian Hamster

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