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Hai cercato: 4,6-Diaminoresorcinol+dihydrochloride


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Codice catalogo: (HUPF0112054)
Fornitore: HUPFER METALLWERKE
Codice articolo fornitore: 0112054
Codice articolo locale: HUPF0112054
Descrizione: Trolley in robust, self-supporting and hygienic design, made of high-quality stainless steel. Ø 25 mm round tube frame with two welded, 1000 ×600 mm deep-drawn shelves with 10 mm high profile edge, lined with sound insulation on the underside, hygienically folded by 35 mm and rebated inwards, designed for easy cleaning. Push bars integrated on both sides into tube frame ensure good manoeuvrability. Trolley with stainless steel panels on three sides and double-wing doors with grip opening and magnetic catch. Four polypropylene disc bumpers serve as bumpers and protect trolley on all sides as well as building-side walls from being damaged. Trolley runs on four swivel casters of which two with total locks, Ø 125 mm, chrome-galvanised housing, plastic caster wheel with roller bearing, failsafe running tread identical to pneumatic casters, with pin fastening.
UOM: 1 * 1 pezzi


Fornitore: MP Biomedicals
Descrizione: 3,3',5,5'-Tetramethylbenzidine is suitable as peroxidase substrate for use in ELISA procedures. The substrate produces a soluble end product that is pale blue in color and can be read spectrophotometrically at 370 or 620 to 650 nm. The TMB reaction may be stopped with 2 M H<sub>2</sub>SO<sub>4</sub> (resulting in a yellow color), and read at 450 nm. A sensitive and specific reagent for the detection of blood, assay of hemoglobin, assay of peroxidases. It is useful in gel staining procedure for low levels of home-associated peroxidases and for enzyme immunoassay of horseradish peroxidase.

Codice catalogo: (BOSSBS-12552R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-12552R-A750
Codice articolo locale: BOSSBS-12552R-A750
Descrizione: Mahogany (MG), originally identified as a protein involved in pigmentation, acts in conjunction with melanocortin receptors to suppress diet-induced obesity. Mahogany contains a single transmembrane domain, and it is expressed in a broad range of tissues, including the hypothalamus and pigment cells. Mutations within the mahogany gene were shown to rescue agouti-lethal-yellow mutant mice from obesity. The extracellular domain of mouse mahogany is the ortholog of the human protein attractin. Attractin (also designated DPPT-L) is a human serum glycoprotein and is a member of the CUB family of cell adhesion and guidance proteins. Attractin is expressed on activated T cells and is released from the cells 48 to 72 hours after activation.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-12551R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-12551R-HRP
Codice articolo locale: BOSSBS-12551R-HRP
Descrizione: Mahogany (MG), originally identified as a protein involved in pigmentation, acts in conjunction with melanocortin receptors to suppress diet-induced obesity. Mahogany contains a single transmembrane domain, and it is expressed in a broad range of tissues, including the hypothalamus and pigment cells. Mutations within the mahogany gene were shown to rescue agouti-lethal-yellow mutant mice from obesity. The extracellular domain of mouse mahogany is the ortholog of the human protein attractin. Attractin (also designated DPPT-L) is a human serum glycoprotein and is a member of the CUB family of cell adhesion and guidance proteins. Attractin is expressed on activated T cells and is released from the cells 48 to 72 hours after activation.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-12552R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-12552R-A555
Codice articolo locale: BOSSBS-12552R-A555
Descrizione: Mahogany (MG), originally identified as a protein involved in pigmentation, acts in conjunction with melanocortin receptors to suppress diet-induced obesity. Mahogany contains a single transmembrane domain, and it is expressed in a broad range of tissues, including the hypothalamus and pigment cells. Mutations within the mahogany gene were shown to rescue agouti-lethal-yellow mutant mice from obesity. The extracellular domain of mouse mahogany is the ortholog of the human protein attractin. Attractin (also designated DPPT-L) is a human serum glycoprotein and is a member of the CUB family of cell adhesion and guidance proteins. Attractin is expressed on activated T cells and is released from the cells 48 to 72 hours after activation.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-12552R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-12552R-HRP
Codice articolo locale: BOSSBS-12552R-HRP
Descrizione: Mahogany (MG), originally identified as a protein involved in pigmentation, acts in conjunction with melanocortin receptors to suppress diet-induced obesity. Mahogany contains a single transmembrane domain, and it is expressed in a broad range of tissues, including the hypothalamus and pigment cells. Mutations within the mahogany gene were shown to rescue agouti-lethal-yellow mutant mice from obesity. The extracellular domain of mouse mahogany is the ortholog of the human protein attractin. Attractin (also designated DPPT-L) is a human serum glycoprotein and is a member of the CUB family of cell adhesion and guidance proteins. Attractin is expressed on activated T cells and is released from the cells 48 to 72 hours after activation.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-12551R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-12551R-CY3
Codice articolo locale: BOSSBS-12551R-CY3
Descrizione: Mahogany (MG), originally identified as a protein involved in pigmentation, acts in conjunction with melanocortin receptors to suppress diet-induced obesity. Mahogany contains a single transmembrane domain, and it is expressed in a broad range of tissues, including the hypothalamus and pigment cells. Mutations within the mahogany gene were shown to rescue agouti-lethal-yellow mutant mice from obesity. The extracellular domain of mouse mahogany is the ortholog of the human protein attractin. Attractin (also designated DPPT-L) is a human serum glycoprotein and is a member of the CUB family of cell adhesion and guidance proteins. Attractin is expressed on activated T cells and is released from the cells 48 to 72 hours after activation.
UOM: 1 * 100 µl


Codice catalogo: (ICNA0520265510)
Fornitore: MP Biomedicals
Codice articolo fornitore: 0520265510
Codice articolo locale: ICNA0520265510
Descrizione: CHROME AZUROL S 1 * 10 g
UOM: 1 * 10 g


Codice catalogo: (PRSI5297)
Fornitore: ProSci Inc.
Codice articolo fornitore: 5297
Codice articolo locale: PRSI5297
Descrizione: TMEM214 Antibody: Transmembrane protein 214 (TMEM214) is a 77kD membrane protein which is widely expressed at high level. The gene encoding this protein maps to chromosome 2, at 2p23.3 TMEM214 interacts with LSM1, an SM-like protein, forming a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing. The detailed function of TMEM214 is still unknown, but a recent study showed that TMEM214 may be used to explore the contribution of human host factors of some infectious diseases such as Dengue fever, West Nile fever and yellow fever. Multiple isoforms of TMEM214 are known to exist.
UOM: 1 * 100 µG


Codice catalogo: (PRSI5299)
Fornitore: ProSci Inc.
Codice articolo fornitore: 5299
Codice articolo locale: PRSI5299
Descrizione: TMEM214 Antibody: Transmembrane protein 214 (TMEM214) is a 77kD membrane protein which is widely expressed at high level. The gene encoding this protein maps to chromosome 2, at 2p23.3 TMEM214 interacts with LSM1, an SM-like protein, forming a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing. The detailed function of TMEM214 is still unknown, but a recent study showed that TMEM214 may be used to explore the contribution of human host factors of some infectious diseases such as Dengue fever, West Nile fever and yellow fever. Multiple isoforms of TMEM214 are known to exist.
UOM: 1 * 100 µG


Codice catalogo: (BOSSBS-11717R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-11717R-CY5
Codice articolo locale: BOSSBS-11717R-CY5
Descrizione: Members of the C1q superfamily have diverse functions that are related to cell adhesion and basement membrane components. CTRP5 (Complement C1q tumor necrosis factor-related protein 5) is a 243 amino acid secreted and membrane-associated protein that contains a collagen-like domain and a C1q domain. CTRP5 is a short-chain collagen that is expressed in retinal pigment epithelium as well as brain, lung, liver and placenta. By forming an extracellular hexagonal lattice, CTRP5 facilitates the adhesion of basal retinal pigment epithelium to Bruch’s membrane, the innermost layer of the choroid. A mutation within the C1q domain of CTRP5 results in abnormal high molecular weight aggregate formation, which alters its structure and interactions. This mutation may result in the presentation of late-onset retinal degeneration (LORD), an autosomal dominant disorder that is characterized by punctate yellow-white deposits in the retinal fundus and night blindness.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11717R)
Fornitore: Bioss
Codice articolo fornitore: BS-11717R
Codice articolo locale: BOSSBS-11717R
Descrizione: Members of the C1q superfamily have diverse functions that are related to cell adhesion and basement membrane components. CTRP5 (Complement C1q tumor necrosis factor-related protein 5) is a 243 amino acid secreted and membrane-associated protein that contains a collagen-like domain and a C1q domain. CTRP5 is a short-chain collagen that is expressed in retinal pigment epithelium as well as brain, lung, liver and placenta. By forming an extracellular hexagonal lattice, CTRP5 facilitates the adhesion of basal retinal pigment epithelium to Bruch’s membrane, the innermost layer of the choroid. A mutation within the C1q domain of CTRP5 results in abnormal high molecular weight aggregate formation, which alters its structure and interactions. This mutation may result in the presentation of late-onset retinal degeneration (LORD), an autosomal dominant disorder that is characterized by punctate yellow-white deposits in the retinal fundus and night blindness.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11717R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-11717R-A350
Codice articolo locale: BOSSBS-11717R-A350
Descrizione: Members of the C1q superfamily have diverse functions that are related to cell adhesion and basement membrane components. CTRP5 (Complement C1q tumor necrosis factor-related protein 5) is a 243 amino acid secreted and membrane-associated protein that contains a collagen-like domain and a C1q domain. CTRP5 is a short-chain collagen that is expressed in retinal pigment epithelium as well as brain, lung, liver and placenta. By forming an extracellular hexagonal lattice, CTRP5 facilitates the adhesion of basal retinal pigment epithelium to Bruch’s membrane, the innermost layer of the choroid. A mutation within the C1q domain of CTRP5 results in abnormal high molecular weight aggregate formation, which alters its structure and interactions. This mutation may result in the presentation of late-onset retinal degeneration (LORD), an autosomal dominant disorder that is characterized by punctate yellow-white deposits in the retinal fundus and night blindness.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11717R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-11717R-A680
Codice articolo locale: BOSSBS-11717R-A680
Descrizione: Members of the C1q superfamily have diverse functions that are related to cell adhesion and basement membrane components. CTRP5 (Complement C1q tumour necrosis factor-related protein 5) is a 243 amino acid secreted and membrane-associated protein that contains a collagen-like domain and a C1q domain. CTRP5 is a short-chain collagen that is expressed in retinal pigment epithelium as well as brain, lung, liver and placenta. By forming an extracellular hexagonal lattice, CTRP5 facilitates the adhesion of basal retinal pigment epithelium to Bruch's membrane, the innermost layer of the choroid. A mutation within the C1q domain of CTRP5 results in abnormal high molecular weight aggregate formation, which alters its structure and interactions. This mutation may result in the presentation of late-onset retinal degeneration (LORD), an autosomal dominant disorder that is characterised by punctate yellow-white deposits in the retinal fundus and night blindness.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11717R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-11717R-CY7
Codice articolo locale: BOSSBS-11717R-CY7
Descrizione: Members of the C1q superfamily have diverse functions that are related to cell adhesion and basement membrane components. CTRP5 (Complement C1q tumor necrosis factor-related protein 5) is a 243 amino acid secreted and membrane-associated protein that contains a collagen-like domain and a C1q domain. CTRP5 is a short-chain collagen that is expressed in retinal pigment epithelium as well as brain, lung, liver and placenta. By forming an extracellular hexagonal lattice, CTRP5 facilitates the adhesion of basal retinal pigment epithelium to Bruch’s membrane, the innermost layer of the choroid. A mutation within the C1q domain of CTRP5 results in abnormal high molecular weight aggregate formation, which alters its structure and interactions. This mutation may result in the presentation of late-onset retinal degeneration (LORD), an autosomal dominant disorder that is characterized by punctate yellow-white deposits in the retinal fundus and night blindness.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-11717R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-11717R-CY3
Codice articolo locale: BOSSBS-11717R-CY3
Descrizione: Members of the C1q superfamily have diverse functions that are related to cell adhesion and basement membrane components. CTRP5 (Complement C1q tumor necrosis factor-related protein 5) is a 243 amino acid secreted and membrane-associated protein that contains a collagen-like domain and a C1q domain. CTRP5 is a short-chain collagen that is expressed in retinal pigment epithelium as well as brain, lung, liver and placenta. By forming an extracellular hexagonal lattice, CTRP5 facilitates the adhesion of basal retinal pigment epithelium to Bruch’s membrane, the innermost layer of the choroid. A mutation within the C1q domain of CTRP5 results in abnormal high molecular weight aggregate formation, which alters its structure and interactions. This mutation may result in the presentation of late-onset retinal degeneration (LORD), an autosomal dominant disorder that is characterized by punctate yellow-white deposits in the retinal fundus and night blindness.
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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