Hai cercato: RuCl2[(S)-dm-segphos®][(S)-daipen]

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

Promo

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

Promo

Codice catalogo: (BOSSBS-11742R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-11742R-A680

Codice articolo locale: BOSSBS-11742R-A680

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

Promo

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

Promo

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

Promo

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

Promo

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

Promo

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

Promo

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

Promo

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

Promo

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

Promo

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

Promo

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

Promo

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

Promo

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

Promo

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