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Product Image-KIMA13125

Probówki do pobierania krwi z antykoagulatem EDTA, próżniowe, Vacutest®

Producent: KIMA SAS DI CHIARIN RENZO
Opis: The test tubes are made from Polyethylene terephthalate (PET). Resistant to mechanical stress, centrifugation, breakage during standard procedures of use and in case of accidental falls. PET is a transparent material which enables the visual inspection of the blood and other biological liquids collected. Labels are made from self-adhesive paper for specific medical use, size 40×20 mm, printed in three colours.

Product Image-720-2691

Probówki do pobierania krwi z heparyną sodową, próżniowe, Vacutest®

Producent: KIMA SAS DI CHIARIN RENZO
Opis: The test tubes are made from Polyethylene terephthalate (PET). Resistant to mechanical stress, centrifugation, breakage during standard procedures of use and in case of accidental fails. PET is a transparent material which enables the visual inspection of the blood and other biological liquids collected. Labels are made from self-adhesive paper for specific medical use, size 40×20 mm, printed in three colours.

Image Unavailable-BOSSBS-9127R-CY7

Anti-CUL7 Rabbit Polyclonal Antibody (Cy7®)

Numer katalogowy: (BOSSBS-9127R-CY7)
Producent: Bioss
Opis: Component of a probable SCF-like E3 ubiquitin-protein ligase complex, which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably plays a role in the degradation of proteins involved in endothelial proliferation and/or differentiation (By similarity). Seems not to promote polyubiquitination and proteasomal degradation of TP53. In vitro, complexes of CUL7 with either CUL9 or FBXW8 or TP53 contain E3 ubiquitin-protein ligase activity.Involvement in disease: Defects in CUL7 are the cause of 3M syndrome type 1 (3M1). An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.
j.m.: 1 * 100 µl
Image Unavailable-BOSSBS-9127R-A555

Anti-CUL7 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Numer katalogowy: (BOSSBS-9127R-A555)
Producent: Bioss
Opis: Component of a probable SCF-like E3 ubiquitin-protein ligase complex, which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably plays a role in the degradation of proteins involved in endothelial proliferation and/or differentiation (By similarity). Seems not to promote polyubiquitination and proteasomal degradation of TP53. In vitro, complexes of CUL7 with either CUL9 or FBXW8 or TP53 contain E3 ubiquitin-protein ligase activity.Involvement in disease: Defects in CUL7 are the cause of 3M syndrome type 1 (3M1). An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.
j.m.: 1 * 100 µl
Image Unavailable-BOSSBS-9127R-HRP

Anti-CUL7 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Numer katalogowy: (BOSSBS-9127R-HRP)
Producent: Bioss
Opis: Component of a probable SCF-like E3 ubiquitin-protein ligase complex, which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably plays a role in the degradation of proteins involved in endothelial proliferation and/or differentiation (By similarity). Seems not to promote polyubiquitination and proteasomal degradation of TP53. In vitro, complexes of CUL7 with either CUL9 or FBXW8 or TP53 contain E3 ubiquitin-protein ligase activity.Involvement in disease: Defects in CUL7 are the cause of 3M syndrome type 1 (3M1). An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.
j.m.: 1 * 100 µl
Image Unavailable-BOSSBS-9127R-CY3

Anti-CUL7 Rabbit Polyclonal Antibody (Cy3®)

Numer katalogowy: (BOSSBS-9127R-CY3)
Producent: Bioss
Opis: Component of a probable SCF-like E3 ubiquitin-protein ligase complex, which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably plays a role in the degradation of proteins involved in endothelial proliferation and/or differentiation (By similarity). Seems not to promote polyubiquitination and proteasomal degradation of TP53. In vitro, complexes of CUL7 with either CUL9 or FBXW8 or TP53 contain E3 ubiquitin-protein ligase activity.Involvement in disease: Defects in CUL7 are the cause of 3M syndrome type 1 (3M1). An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.
j.m.: 1 * 100 µl
Image Unavailable-BOSSBS-9127R-A647

Anti-CUL7 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Numer katalogowy: (BOSSBS-9127R-A647)
Producent: Bioss
Opis: Component of a probable SCF-like E3 ubiquitin-protein ligase complex, which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably plays a role in the degradation of proteins involved in endothelial proliferation and/or differentiation (By similarity). Seems not to promote polyubiquitination and proteasomal degradation of TP53. In vitro, complexes of CUL7 with either CUL9 or FBXW8 or TP53 contain E3 ubiquitin-protein ligase activity.Involvement in disease: Defects in CUL7 are the cause of 3M syndrome type 1 (3M1). An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.
j.m.: 1 * 100 µl
Image Unavailable-BOSSBS-9127R

Anti-CUL7 Rabbit Polyclonal Antibody

Numer katalogowy: (BOSSBS-9127R)
Producent: Bioss
Opis: Component of a probable SCF-like E3 ubiquitin-protein ligase complex, which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably plays a role in the degradation of proteins involved in endothelial proliferation and/or differentiation (By similarity). Seems not to promote polyubiquitination and proteasomal degradation of TP53. In vitro, complexes of CUL7 with either CUL9 or FBXW8 or TP53 contain E3 ubiquitin-protein ligase activity.Involvement in disease: Defects in CUL7 are the cause of 3M syndrome type 1 (3M1). An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.
j.m.: 1 * 100 µl
Image Unavailable-BOSSBS-9127R-A680

Anti-Cullin 7 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Numer katalogowy: (BOSSBS-9127R-A680)
Producent: Bioss
Opis: Component of a probable SCF-like E3 ubiquitin-protein ligase complex, which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably plays a role in the degradation of proteins involved in endothelial proliferation and/or differentiation (By similarity). Seems not to promote polyubiquitination and proteasomal degradation of TP53. <i>in vitro</i>, complexes of CUL7 with either CUL9 or FBXW8 or TP53 contain E3 ubiquitin-protein ligase activity.Involvement in disease: Defects in CUL7 are the cause of 3M syndrome type 1 (3M1). An autosomal recessive disorder characterised by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.
j.m.: 1 * 100 µl
Image Unavailable-BOSSBS-9127R-A488

Anti-CUL7 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Numer katalogowy: (BOSSBS-9127R-A488)
Producent: Bioss
Opis: Component of a probable SCF-like E3 ubiquitin-protein ligase complex, which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably plays a role in the degradation of proteins involved in endothelial proliferation and/or differentiation (By similarity). Seems not to promote polyubiquitination and proteasomal degradation of TP53. In vitro, complexes of CUL7 with either CUL9 or FBXW8 or TP53 contain E3 ubiquitin-protein ligase activity.Involvement in disease: Defects in CUL7 are the cause of 3M syndrome type 1 (3M1). An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.
j.m.: 1 * 100 µl
Product Image-720-2732

Probówki weterynaryjne do pobierania krwi z aktywatorem skrzepu, próżnia, Vacutest®

Producent: KIMA SAS DI CHIARIN RENZO
Opis: The test tubes are made from polyethylene terephthalate (PET). Resistant to mechanical stress, centrifugation, breakage during standard procedures of use and in case of accidental falls. PET is a transparent material which enables the visual inspection of the blood and other biological liquids collected. Labels are made from self-adhesive paper for specific medical use (40×20 mm), printed in three colours.

Image Unavailable-BOSSBS-9127R-CY5.5

Anti-CUL7 Rabbit Polyclonal Antibody (Cy5.5®)

Numer katalogowy: (BOSSBS-9127R-CY5.5)
Producent: Bioss
Opis: Component of a probable SCF-like E3 ubiquitin-protein ligase complex, which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably plays a role in the degradation of proteins involved in endothelial proliferation and/or differentiation (By similarity). Seems not to promote polyubiquitination and proteasomal degradation of TP53. In vitro, complexes of CUL7 with either CUL9 or FBXW8 or TP53 contain E3 ubiquitin-protein ligase activity.Involvement in disease: Defects in CUL7 are the cause of 3M syndrome type 1 (3M1). An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.
j.m.: 1 * 100 µl
Image Unavailable-BOSSBS-9127R-FITC

Anti-CUL7 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Numer katalogowy: (BOSSBS-9127R-FITC)
Producent: Bioss
Opis: Component of a probable SCF-like E3 ubiquitin-protein ligase complex, which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably plays a role in the degradation of proteins involved in endothelial proliferation and/or differentiation (By similarity). Seems not to promote polyubiquitination and proteasomal degradation of TP53. In vitro, complexes of CUL7 with either CUL9 or FBXW8 or TP53 contain E3 ubiquitin-protein ligase activity.Involvement in disease: Defects in CUL7 are the cause of 3M syndrome type 1 (3M1). An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.
j.m.: 1 * 100 µl
Product Image-720-2730

Probówki do pobierania krwi z aktywatorem krzepnięcia, próżniowe, Vacutest®

Producent: KIMA SAS DI CHIARIN RENZO
Opis: The test tubes are made from Polyethylene terephthalate (PET). Resistant to mechanical stress, centrifugation, breakage during standard procedures of use and in case of accidental falls. PET is a transparent material which enables the visual inspection of the blood and other biological liquids collected. Labels are made from self-adhesive paper for specific medical use, size 40×20 mm, printed in three colours.

Image Unavailable-ICNA04818048

Fenol, white solid, Ultrapure

Numer katalogowy: (ICNA04818048)
Producent: MP Biomedicals
Opis: Phenol is useful for extraction of viral, plasmid and phage DNAs, and to solubilise and dissociate proteins. It is used as a general disinfectant, either in solution or mixed with slaked lime, etc., for toilets, stables, cesspools, floors, drains, etc.; for the manufacture of colorless or light-colored artificial resins, many medical and industrial organic compounds and dyes; as a reagent in chemical analysis. Aqueous solutions are used as topical anesthetic; topical antiseptic; topical antipruritic. Phenol is used in DNA extractions for removing protein.
j.m.: 1 * 500 g
Image Unavailable-PRSI33-646

Anti-MLANA Rabbit Polyclonal Antibody

Numer katalogowy: (PRSI33-646)
Producent: ProSci Inc.
Opis: MART-1/Melan-A is a protein antigen that is found on the surface of melanocytes. Antibodies against the antigen are used in the medical specialty of anatomic pathology in order to recognize cells of melanocytic differentiation, useful for the diagnosis of a melanoma. The MART-1/Melan-A antigen is specific for the melanocyte lineage, found in normal skin, the retina, and melanocytes, but not in other normal tissues. It is thus useful as a marker for melanocytic tumors (melanomas) with the caveat that it is normally found in benign nevi as well. [Wiki].
j.m.: 1 * 100 µG
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Zapasy tego artykułu są ograniczone, ale możliwe, że jest on dostępny w pobliskim magazynie. Upewnij się, że jesteś zalogowany na stronie, aby móc sprawdzić dostępność zapasów. Jeśli call ciągle się wyświetla i potrzebujesz pomocy, zadzwoń na 58 323 82 00.
Ten produkt jest ograniczony w dostępie i można go zamówić tylko przy użyciu zaaprobowanego konta. Jeśli potrzebujesz pomocy, napisz do Działu Prawnego VWR na tomasz.chrobak@pl.vwr.com
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Wybrany produkt został wycofany - sprzedaż do wyczerpania zapasów. Dostępne zamienniki można znaleźć poprzez wpisanie powyższego numeru katalogowego VWR w okno wyszukiwarki. Jeśli potrzebujesz dalszej pomocy, prosimy o kontakt z Działem Doradztwa Produktowego pod numerem telefonu 58 3238 220.
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