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Proflavine hydrochloride (3,6-diaminoacridine hydrochloride)

Codice catalogo: (ACRO465860050)
Fornitore: Thermo Fisher Scientific
Codice articolo fornitore: 465860050
Codice articolo locale: ACRO465860050
Descrizione: Proflavine hydrochloride (3,6-diaminoacridine hydrochloride)
UOM: 1 * 5 g
Image Unavailable-TCIAA0133-5G

9-Acridone ≥98.0% (by HPLC, total nitrogen)

Fornitore: TCI
Descrizione: 9-Acridone ≥98.0% (by HPLC, total nitrogen)

Image Unavailable-TCIAD4780-200MG

N,N'-Dibutylquinacridone ≥98.0% (by HPLC, total nitrogen)

Fornitore: TCI
Descrizione: N,N'-Dibutylquinacridone ≥98.0% (by HPLC, total nitrogen)

Product Image-PIER87760

Dialysis flasks, Slide-A-Lyzer™

Fornitore: Thermo Fisher Scientific
Descrizione: These dialysis flasks facilitate simple and effective removal of buffer salts and small contaminants from proteins and other macromolecules in sample volumes up to 250 ml.

Image Unavailable-TCIAD2687-1G

N,N'-Dimethylquinacridone ≥96.0% (by HPLC)

Fornitore: TCI
Descrizione: N,N'-Dimethylquinacridone ≥96.0% (by HPLC)

Image Unavailable-BOSSBS-9847R-A750

Anti-AE2 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Codice catalogo: (BOSSBS-9847R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-9847R-A750
Codice articolo locale: BOSSBS-9847R-A750
Descrizione: Primary canalicular bile undergoes a process of fluidization and alkalinization along the biliary tract that is influenced by several factors, including hormones, innervation/neuropeptides and biliary constituents. The excretion of bicarbonate at both the canaliculi and the bile ducts is an important contributor to the generation of bile-salt independent flow. Bicarbonate is secreted from hepatocytes and cholangiocytes through parallel mechanisms, which involve chloride efflux through activation of chloride channels and further bicarbonate secretion via AE2 (also designated SLC4A2)-mediated chloride/bicarbonate exchange. The AE2 protein regulates pH, chloride concentration, cell volume and transepithelial ion transport in many tissues. Gene silencing of AE2 causes a marked inhibition of unstimulated and secretin-stimulated chloride/bicarbonate exchange, which maintains the bile acid pool that is crucial for secretin to induce bicarbonate-rich choleresis.
UOM: 1 * 100 µl
Image Unavailable-TCIAD3227-1G

N,N'-Dimethylquinacridone ≥96.0% (by HPLC), purified by sublimation

Codice catalogo: (TCIAD3227-1G)
Fornitore: TCI
Codice articolo fornitore: D3227-1G
Codice articolo locale: TCIAD3227-1G
Descrizione: N,N'-Dimethylquinacridone ≥96.0% (by HPLC), purified by sublimation
UOM: 1 * 1 g
Image Unavailable-BOSSBS-13627R-FITC

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

Codice catalogo: (BOSSBS-13627R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-13627R-FITC
Codice articolo locale: BOSSBS-13627R-FITC
Descrizione: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13627R-CY5

Anti-CLCNKB Rabbit Polyclonal Antibody (Cy5®)

Codice catalogo: (BOSSBS-13627R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-13627R-CY5
Codice articolo locale: BOSSBS-13627R-CY5
Descrizione: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13627R-HRP

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

Codice catalogo: (BOSSBS-13627R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-13627R-HRP
Codice articolo locale: BOSSBS-13627R-HRP
Descrizione: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13627R-A350

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

Codice catalogo: (BOSSBS-13627R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-13627R-A350
Codice articolo locale: BOSSBS-13627R-A350
Descrizione: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13627R-A647

Anti-CLCNKB Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Codice catalogo: (BOSSBS-13627R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-13627R-A647
Codice articolo locale: BOSSBS-13627R-A647
Descrizione: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-10307R-A680

Anti-Chloride Channel 5 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Codice catalogo: (BOSSBS-10307R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-10307R-A680
Codice articolo locale: BOSSBS-10307R-A680
Descrizione: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport and maintain cellular volume. The genes encoding human CLC-1 through CLC-7 map to chromosomes 7q32, 3q28, 4q32, Xp22.3, Xp11.23-p11.22, 1p36 and 16p13, respectively. CLC1 is highly expressed in skeletal muscle. Mutations in the gene encoding CLC1 lead to myotonia, an inheritable disorder characterised by muscle stiffness and renal salt wasting. CLC2 is highly expressed in the epithelia of several organs including lung, which suggests CLC2 may be a possible therapeutic target for cystic fibrosis. CLC3 expression is particularly abundant in neuronal tissue, while CLC4 expression is evident in skeletal and cardiac muscle as well as brain. Mutations in the gene encoding CLC5 lead to Dent's disease, a renal disorder characterised by proteinuria and hypercalciuria. CLC6 and CLC7 are broadly expressed in several tissues including testis, kidney, brain and muscle.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13627R-CY3

Anti-CLCNKB Rabbit Polyclonal Antibody (Cy3®)

Codice catalogo: (BOSSBS-13627R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-13627R-CY3
Codice articolo locale: BOSSBS-13627R-CY3
Descrizione: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13627R-A680

Anti-CLCNKB Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Codice catalogo: (BOSSBS-13627R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-13627R-A680
Codice articolo locale: BOSSBS-13627R-A680
Descrizione: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter?s syndrome which is characterized by renal salt-wasting and low blood pressure.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-10307R-A750

Anti-Chloride Channel 5 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Codice catalogo: (BOSSBS-10307R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-10307R-A750
Codice articolo locale: BOSSBS-10307R-A750
Descrizione: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport and maintain cellular volume. The genes encoding human CLC-1 through CLC-7 map to chromosomes 7q32, 3q28, 4q32, Xp22.3, Xp11.23-p11.22, 1p36 and 16p13, respectively. CLC1 is highly expressed in skeletal muscle. Mutations in the gene encoding CLC1 lead to myotonia, an inheritable disorder characterised by muscle stiffness and renal salt wasting. CLC2 is highly expressed in the epithelia of several organs including lung, which suggests CLC2 may be a possible therapeutic target for cystic fibrosis. CLC3 expression is particularly abundant in neuronal tissue, while CLC4 expression is evident in skeletal and cardiac muscle as well as brain. Mutations in the gene encoding CLC5 lead to Dent's disease, a renal disorder characterised by proteinuria and hypercalciuria. CLC6 and CLC7 are broadly expressed in several tissues including testis, kidney, brain and muscle.
UOM: 1 * 100 µl
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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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