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Image Unavailable-ENZOBMLCM1120500

clopamide ≥98% (by HPLC)

Numer katalogowy: (ENZOBMLCM1120500)
Producent: ENZO LIFE SCIENCES
Opis: Clinically useful diuretic. Clopamide selectively inhibits the chloride the sodium chloride cotransporter.
j.m.: 1 * 500 mg

New Product


Product Image-HOIT109758

Czepki, włóknina PP

Numer katalogowy: (HOIT109758)
Producent: HUBEI ORIENT INTL TRADING
Opis: Disposable mob caps made from non woven PP.
j.m.: 1 * 1.000 SZT

Nowy przejrzysty widok dla europejskich klientów

Czy wiesz, że wprowadziliśmy nową, ulepszoną widoczność lokalizacji zapasów przy realizacji zamówienia?

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Udoskonalenia w zakresie lokalizacji zapasów magazynowych

Product Image-HOIT4021W52BDAC3XL

Kombinezon z kapturem i bez osłony stóp, PP

Producent: HUBEI ORIENT INTL TRADING
Opis: These disposable overalls are made from non woven PP. Ideal for non critical applications in industrial, clinical or food processing environments.

Product Image-RATI7000260

Torebki do czyszczenia, ratiolab

Producent: RATIOLAB
Opis: All-purpose PE bags with self-adhesive strip for clinical and laboratory use.

Image Unavailable-BOSSBS-4807R-A750

Anti-ATXN3L Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Numer katalogowy: (BOSSBS-4807R-A750)
Producent: Bioss
Opis: Defects in ATXN3 are the cause of spinocerebellar ataxia type 3 (SCA3) ; also known as Machado-Joseph disease (MJD). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA3 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterised by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. The molecular defect in SCA3 is the a CAG repeat expansion in ATXN3 coding region. Longer expansions result in earlier onset and more severe clinical manifestations of the disease.
j.m.: 1 * 100 µl
Image Unavailable-BOSSBS-4807R-HRP

Anti-ATXN3L Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Numer katalogowy: (BOSSBS-4807R-HRP)
Producent: Bioss
Opis: Defects in ATXN3 are the cause of spinocerebellar ataxia type 3 (SCA3) ; also known as Machado-Joseph disease (MJD). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA3 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. The molecular defect in SCA3 is the a CAG repeat expansion in ATXN3 coding region. Longer expansions result in earlier onset and more severe clinical manifestations of the disease.
j.m.: 1 * 100 µl
Product Image-LIOF96147

Testy lateksowe

Numer katalogowy: (LIOF96147)
Producent: LIOFILCHEM
Opis: Identification of the main pathogenic microorganisms directly from clinical specimens.
j.m.: 1 * 1 SZT
Product Image-630-3168

Mikroskopy pionowe, DM 1000 LED

Producent: LEICA MICROSYSTEMS
Opis: The DM1000 LED laboratory microscope is perfect for clinical laboratory applications; histology, cytology, haematology and pathology.

Image Unavailable-ICNA091003122

Medium do hodowli komórek, sproszkowane, pożywka Eagle'a (BME) modyfikowana

Numer katalogowy: (ICNA091003122)
Producent: MP Biomedicals
Opis: Basal Medium Eagle is suited for the isolation and cultivation of non-fastidious and fastidious microorganisms from a variety of clinical and non-clinical specimens. It can also be used as a selective isolation medium by adding antimicrobial agents.
j.m.: 1 * 10 L
Product Image-631-1075

VWR® Q Path® Slide Holders

Producent: VWR Collection
Opis: Slide holders designed for applications in clinical cytology.

Product Image-113-9220

Czepki Bouffant, PP

Producent: HUBEI ORIENT INTL TRADING
Opis: Disposable bouffant caps made from non woven PP. Ideal for use in non hazardous environments.

Image Unavailable-BOSSBS-4807R-A350

Anti-ATXN3L Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Numer katalogowy: (BOSSBS-4807R-A350)
Producent: Bioss
Opis: Defects in ATXN3 are the cause of spinocerebellar ataxia type 3 (SCA3) ; also known as Machado-Joseph disease (MJD). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA3 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. The molecular defect in SCA3 is the a CAG repeat expansion in ATXN3 coding region. Longer expansions result in earlier onset and more severe clinical manifestations of the disease.
j.m.: 1 * 100 µl
Image Unavailable-BOSSBS-4807R-A555

Anti-ATXN3L Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Numer katalogowy: (BOSSBS-4807R-A555)
Producent: Bioss
Opis: Defects in ATXN3 are the cause of spinocerebellar ataxia type 3 (SCA3) ; also known as Machado-Joseph disease (MJD). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA3 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. The molecular defect in SCA3 is the a CAG repeat expansion in ATXN3 coding region. Longer expansions result in earlier onset and more severe clinical manifestations of the disease.
j.m.: 1 * 100 µl
Image Unavailable-BOSSBS-4807R-CY5.5

Anti-ATXN3L Rabbit Polyclonal Antibody (Cy5.5®)

Numer katalogowy: (BOSSBS-4807R-CY5.5)
Producent: Bioss
Opis: Defects in ATXN3 are the cause of spinocerebellar ataxia type 3 (SCA3) ; also known as Machado-Joseph disease (MJD). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA3 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. The molecular defect in SCA3 is the a CAG repeat expansion in ATXN3 coding region. Longer expansions result in earlier onset and more severe clinical manifestations of the disease.
j.m.: 1 * 100 µl
Image Unavailable-BOSSBS-4807R-CY5

Anti-ATXN3L Rabbit Polyclonal Antibody (Cy5®)

Numer katalogowy: (BOSSBS-4807R-CY5)
Producent: Bioss
Opis: Defects in ATXN3 are the cause of spinocerebellar ataxia type 3 (SCA3) ; also known as Machado-Joseph disease (MJD). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA3 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. The molecular defect in SCA3 is the a CAG repeat expansion in ATXN3 coding region. Longer expansions result in earlier onset and more severe clinical manifestations of the disease.
j.m.: 1 * 100 µl
Image Unavailable-OXOIS611430-6

Test immunofluorescencyjny, IMAGEN™

Producent: THERMO FISHER DIAGNOSTICS
Opis: IMAGEN™ is a qualitative direct immunofluorescence test used for detection and confirmation of the presence of virus in cell culture or in clinical specimen.

Cena wymaga potwierdzenia u dostawcy
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.
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
Do zakupu tego produktu może być potrzebna dodatkowa dokumentacja. Przedstawiciel VWR skontaktuje się z Tobą w razie potrzeby.
Ten produkt jest zablokowany na stronie internetowej. W celu zamówienia, skontaktuj się z Działem Obsługi Klienta.
Produkt oryginalny został wycofany. Dostępny jest wskazny zamiennik .
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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