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Image Unavailable-BOSSBS-9652R-CY5.5

Anti-LDLRAD4 Rabbit Polyclonal Antibody (Cy5.5®)

Codice catalogo: (BOSSBS-9652R-CY5.5)
Fornitore: Bioss
Codice articolo fornitore: BS-9652R-CY5.5
Codice articolo locale: BOSSBS-9652R-CY5.5
Descrizione: C18orf1 is a 306 amino acid single-pass membrane protein that contains one LDL-receptor class A domain and belongs to the PMEPA1 family. C18orf1 exists as five alternatively spliced isoforms that display selective expression and are encoded by a gene that maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-4944R-A488

Anti-SETBP1 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Codice catalogo: (BOSSBS-4944R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-4944R-A488
Codice articolo locale: BOSSBS-4944R-A488
Descrizione: SETBP1 (SET binding protein 1), also known as SEB, is a 1,542 amino acid nuclear protein that contains three AT hook DNA-binding domains, one SKI homology region and a C-terminal SET-binding domain, which is followed by three PPLPPPPP repeats. SETBP1 may be involved in SET-related tumorigenesis and leukemogenesis by regulating the transforming activity of SKI in the nucleus or suppressing SET function. As a widely expressed protein, SETBP1 is encoded by a gene that maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9652R-A647

Anti-LDLRAD4 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Codice catalogo: (BOSSBS-9652R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-9652R-A647
Codice articolo locale: BOSSBS-9652R-A647
Descrizione: C18orf1 is a 306 amino acid single-pass membrane protein that contains one LDL-receptor class A domain and belongs to the PMEPA1 family. C18orf1 exists as five alternatively spliced isoforms that display selective expression and are encoded by a gene that maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
UOM: 1 * 100 µl
Product Image-IKAA20008820

Homogenisers, T 25 digital LR

Codice catalogo: (IKAA20008820)
Fornitore: IKA
Codice articolo fornitore: 20008820
Codice articolo locale: IKAA20008820
Descrizione: Powerful disperser for volumes ranging from 1 to 2000 ml (H2O) with digital speed display. The wide speed range of 600 to 25000 rpm facilitates work with high circumferential speeds. An extensive selection of dispersing shafts makes multiple applications possible. The application range includes homogenisation and dispersion tasks for use under vacuum in the IKA laboratory reactors.
UOM: 1 * 1 pezzi
Product Image-BINZ113358

High purity qualitative filter paper

Fornitore: Ahlstrom-Munksjö
Descrizione: Ahlstrom-Munksjö’s qualitative grades of filter paper are recommended for use in analytical methods which determine or identify particulate constituents of a mixture irrespective of the amount present. Qualitative filter papers are often used in routine separation work that still requires high purity and consistent performance. These filter papers covers a wide range of laboratory applications, as liquids clarification, qualitative analytical separations for precipitates and buffers filtration, and are also used for soil analysis and in food and beverage testing. Wet-strengthened grades contain a reinforcement agent that increases their resistance to rupture when wet, such as in vacuum filtration, and their resistance when filtering acidic solutions.

Product Image-663-0295

Conduttimetri, da banco, FiveEasy™ F30/FiveEasy™ Plus FP30

Fornitore: Mettler - Toledo
Descrizione: Strumenti da banco per misurazioni della conducibilità di alta qualità al semplice tocco di un pulsante. Il funzionamento intuitivo, il design elegante e le semplici funzioni di esportazione dei dati rendono questi misuratori semplici da impostare e utilizzare. Ideali per l'impiego nella lavorazione di alimenti e bibite, nel settore agricolo, ambientale, nell'industria e per scopi didattici.

Product Image-181-0235

VWR®, Pompe da vuoto compatte per filtrazione ed estrazione in fase solida

Fornitore: VACUUBRAND
Descrizione: La filtrazione sotto vuoto è una delle applicazioni più comuni utilizzate per la preparazione dei campioni in chimica, microbiologia, controllo delle acque reflue e in altri processi di analisi. Le pompe a membrana compatte VP 100 e VP 100 C assicurano prestazioni elevate e facilità d'uso e rappresentano la soluzione ideale per filtrazioni singole e multiple.

Image Unavailable-BUCH11100V211

Rotary evaporators, Rotavapor® R-100 Essential

Fornitore: BUCHI
Descrizione: The R-100 is available as a stand-alone unit or as a complete ready to use kit (Essential Solution kit). The Essential Solution kits provide an economical and complete high-end evaporation solution. The kits include a Rotavapor® R-100 evaporator, a regulated vacuum pump (V-100), an interface (I-100) and an optional chiller (F-100 / F-105) to cover all the main evaporation applications efficiently.

Image Unavailable-BOSSBS-4944R-FITC

Anti-SETBP1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Codice catalogo: (BOSSBS-4944R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-4944R-FITC
Codice articolo locale: BOSSBS-4944R-FITC
Descrizione: SETBP1 (SET binding protein 1), also known as SEB, is a 1,542 amino acid nuclear protein that contains three AT hook DNA-binding domains, one SKI homology region and a C-terminal SET-binding domain, which is followed by three PPLPPPPP repeats. SETBP1 may be involved in SET-related tumorigenesis and leukemogenesis by regulating the transforming activity of SKI in the nucleus or suppressing SET function. As a widely expressed protein, SETBP1 is encoded by a gene that maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-4944R-CY3

Anti-SETBP1 Rabbit Polyclonal Antibody (Cy3®)

Codice catalogo: (BOSSBS-4944R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-4944R-CY3
Codice articolo locale: BOSSBS-4944R-CY3
Descrizione: SETBP1 (SET binding protein 1), also known as SEB, is a 1,542 amino acid nuclear protein that contains three AT hook DNA-binding domains, one SKI homology region and a C-terminal SET-binding domain, which is followed by three PPLPPPPP repeats. SETBP1 may be involved in SET-related tumorigenesis and leukemogenesis by regulating the transforming activity of SKI in the nucleus or suppressing SET function. As a widely expressed protein, SETBP1 is encoded by a gene that maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9652R-CY7

Anti-LDLRAD4 Rabbit Polyclonal Antibody (Cy7®)

Codice catalogo: (BOSSBS-9652R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-9652R-CY7
Codice articolo locale: BOSSBS-9652R-CY7
Descrizione: C18orf1 is a 306 amino acid single-pass membrane protein that contains one LDL-receptor class A domain and belongs to the PMEPA1 family. C18orf1 exists as five alternatively spliced isoforms that display selective expression and are encoded by a gene that maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9652R-A555

Anti-LDLRAD4 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Codice catalogo: (BOSSBS-9652R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-9652R-A555
Codice articolo locale: BOSSBS-9652R-A555
Descrizione: C18orf1 is a 306 amino acid single-pass membrane protein that contains one LDL-receptor class A domain and belongs to the PMEPA1 family. C18orf1 exists as five alternatively spliced isoforms that display selective expression and are encoded by a gene that maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9258R-CY5

Anti-RNF165 Rabbit Polyclonal Antibody (Cy5®)

Codice catalogo: (BOSSBS-9258R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-9258R-CY5
Codice articolo locale: BOSSBS-9258R-CY5
Descrizione: The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in protein-protein interactions and protein-DNA interactions. Specifically, they are thought to be involved in the ubiquitination pathway of protein degradation. RNF165 (RING finger protein 165) is a 346 amino acid protein that contains one RING-type zinc finger. Via its RING-type zinc finger, RNF165 may play a role in transcriptional regulation and protein degradation events. The gene encoding RNF165 maps to human chromosome 18, which houses over 300 genes, including Trisomy 18, or Edwards syndrome, the second most common trisomy after Downs syndrome. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are also associated with chromosome 18.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9212R-FITC

Anti-SERPINB11 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Codice catalogo: (BOSSBS-9212R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-9212R-FITC
Codice articolo locale: BOSSBS-9212R-FITC
Descrizione: The serine proteinase inhibitors (serpins) compose a superfamily of proteins with a diverse set of functions, including the control of blood coagulation, complement activation, programmed cell death and development. Serpins are secreted glycoproteins that contain a stretch of peptide that mimics a true substrate for a corresponding serine protease. SerpinB11 (serpin peptidase inhibitor, clade B (ovalbumin), member 11), also known as EPIPIN or SERPIN11, is a 392 amino acid cytoplasmic protein that belongs to the Ov-serpin subfamily and serpin family. Like other members of the serpin family, SerpinB11 has been identified as a noninhibitory intracellular protein. The gene encoding SerpinB11 maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
UOM: 1 * 100 µl
Product Image-466-0341

Stufe ad alta capacità di carico, Heratherm™ serie General Protocol e Advanced Protocol

Fornitore: Thermo Fisher Scientific
Descrizione: Heratherm™ large capacity ovens were designed for larger samples or high sample volume. All models have a large, easy to view, vacuum fluorescence display and simple to use touch button operation which is controlled by a microprocessor and automatic over-temperature alarm system to protect samples. All units are available in convenient 230 V version - no special connection required.

Image Unavailable-BOSSBS-4944R-A350

Anti-SETBP1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Codice catalogo: (BOSSBS-4944R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-4944R-A350
Codice articolo locale: BOSSBS-4944R-A350
Descrizione: SETBP1 (SET binding protein 1), also known as SEB, is a 1,542 amino acid nuclear protein that contains three AT hook DNA-binding domains, one SKI homology region and a C-terminal SET-binding domain, which is followed by three PPLPPPPP repeats. SETBP1 may be involved in SET-related tumorigenesis and leukemogenesis by regulating the transforming activity of SKI in the nucleus or suppressing SET function. As a widely expressed protein, SETBP1 is encoded by a gene that maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
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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