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Product Image-ERLAAA616A00011A21

Ductless filtering fume hoods, Captair® Smart 391

Katalogové číslo: (ERLAAA616A00011A21)
Dodavatel: ERLAB CAPTAIRE
Popis: The new Captair® Smart ductless filtering hoods are designed with a simple and innovative way of communication. Smart Technology, simple and intuitive communication by light indicates the status of the hood. A simple light pattern will indicate if the airflow is compromised, if there is a fan failure or in case of a filter breakthrough.
Please complete the quote request to enable us to assist you in finding the right unit for your application.
https://cz.cmd2.vwr.com/bin/public/fc/main?f=Y5&pimid=17327607
Měrná jednotka: 1 * 1 KS

New Product


Product Image-MOTI1101010100151

LED illuminator, VI-LED vertical illuminator

Katalogové číslo: (MOTI1101010100151)
Dodavatel: MOTIC
Popis: VI-LED vertical illuminator enables on-axis observation and documentation, and is specially designed for Motic SMZ-161 and SMZ-171. VI-LED directs light from the 3 W LED down through the objective onto the specimen. It is powered by the switching power supply for worldwide use (100 to 240 V). Ideal for the observation of particularly smooth, specular surfaces and highly reflective specimens such as integrated circuits, semi-conductor wafers, polished metal parts, solder balls, or magnetic recording heads.
Měrná jednotka: 1 * 1 KS

Nové řešení transparentnosti pro evropské zákazníky

Všimli jste si naší nově zlepšené viditelnosti rozmístění zásob u pokladny?

Zjistěte více

Zlepšení rozmístění zásob

Product Image-460-0272

Digital block heaters, QBD and QBH

Dodavatel: GRANT INSTRUMENTS
Popis: Compact digital block heaters with choice of models for 1 or 2 or 4 interchangeable blocks. Units feature an LED temperature display, easy to use interactive user interface for fast and accurate set up. Variable high and low temperature alarms can be set to within 0,5 °C of the set point. Heaters are made from cool wall aluminium and chemically resistant plastic, have a low profile, a sloping fascia for ease of use, off-set adjustment for high accuracy operating temperatures and 0,1 °C display resolution.

Product Image-BOHLR1320-45

System waste caps, b.safe

Dodavatel: Bohlender
Popis: b.safe waste tubes can be connected to the canister by means of these b.safe system waste caps and solvents can be collected safely. Solvent vapours are held back by the exhaust filter with activated carbon or can be led to the hood by means of a venting hose.

Image Unavailable-ENZOADI905015100

Anti-8-ISO-PGF2 alpha Rabbit Polyclonal Antibody

Katalogové číslo: (ENZOADI905015100)
Dodavatel: ENZO LIFE SCIENCES
Popis: Prostaglandin F2alpha (PGF2alpha) is formed in a variety of cells from PGH2, which itself is synthesized from arachidonic acid by the enzyme prostaglandin synthetase. PGF2alpha is often viewed as an antagonist to PGE2 due to their opposing effects on various tissues. PGF2alpha is a potent bronchoconstrictor and has been implicated in asthma attacks. PGF2alpha is also involved in reproductive functions including corpus luteum regulation, uterine contractions, and sperm motility. This has led to its use in terminating pregnancies and inducing labor at term. High levels of PGF2alpha have also been associated with preeclampsia.
Měrná jednotka: 1 * 100 µl

New Product


Image Unavailable-BOSSBS-7341R-A680

Anti-C16orf72 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Katalogové číslo: (BOSSBS-7341R-A680)
Dodavatel: Bioss
Popis: Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterised by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The C16orf72 gene product has been provisionally designated C16orf72 pending further characterisation.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-9470R-CY5.5

Anti-MEF2B Rabbit Polyclonal Antibody (Cy5.5®)

Katalogové číslo: (BOSSBS-9470R-CY5.5)
Dodavatel: Bioss
Popis: The myocyte enhancer factor-2 (MEF-2) family of transcription factors associate with co-repessors or co-activators to regulate development and function of T cells, neuronal cells, and muscle cells. Four family members, termed MEF-2A, -2B, -2C, and -2D, arise from alternatively spliced transcripts. These members bind as homo- and heterodimers to the MEF-2 site in the promoter region of affected genes. Differential regulation in the expression of the four transcripts implies functional distinction for each during embryogenesis and development. The process of differentiation from mesodermal precursor cells to myoblasts has led to the discovery of a variety of tissue-specific factors that regulate muscle gene expression. The myogenic basic helix-loop-helix proteins, including MyoD, myogenin, Myf-5, and MRF4, are one class of identified factors. The MEF-2 family represents a second class of DNA binding regulatory proteins. Each of these proteins binds to the MEF-2 target DNA sequence present in the regulatory regions of many muscle-specific genes.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-9729R-A350

Anti-FAM96B Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Katalogové číslo: (BOSSBS-9729R-A350)
Dodavatel: Bioss
Popis: Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The FAM96B gene product has been provisionally designated FAM96B pending further characterization.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-11130R-A750

Anti-VAT1L/KIAA1576 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Katalogové číslo: (BOSSBS-11130R-A750)
Dodavatel: Bioss
Popis: Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterised by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumour growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The KIAA1576 gene product has been provisionally designated KIAA1576 pending further characterisation.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-11130R-A680

Anti-VAT1L/KIAA1576 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Katalogové číslo: (BOSSBS-11130R-A680)
Dodavatel: Bioss
Popis: Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterised by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumour growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The KIAA1576 gene product has been provisionally designated KIAA1576 pending further characterisation.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-9629R-A350

Anti-C16orf7 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Katalogové číslo: (BOSSBS-9629R-A350)
Dodavatel: Bioss
Popis: Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-9629R-A555

Anti-C16orf7 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Katalogové číslo: (BOSSBS-9629R-A555)
Dodavatel: Bioss
Popis: Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-9023R-A488

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

Katalogové číslo: (BOSSBS-9023R-A488)
Dodavatel: Bioss
Popis: Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. alternatively splicing events.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-9023R-FITC

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

Katalogové číslo: (BOSSBS-9023R-FITC)
Dodavatel: Bioss
Popis: Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. alternatively splicing events.
Měrná jednotka: 1 * 100 µl
Product Image-ERLAAA636A00011A21

Ductless filtering fume hoods, Captair® Smart 392

Katalogové číslo: (ERLAAA636A00011A21)
Dodavatel: ERLAB CAPTAIRE
Popis: The Captair® Smart ductless filtering hoods are designed with a simple and innovative way of communication. Smart Technology, simple and intuitive communication by light indicates the status of the hood.
Please complete the quote request to enable us to assist you in finding the right unit for your application.
https://cz.cmd2.vwr.com/bin/public/fc/main?f=Y5&pimid=20532258
Měrná jednotka: 1 * 1 KS

New Product


Product Image-ERLAAA666A00011A21

Ductless filtering fume hoods, Captair® Smart 714

Katalogové číslo: (ERLAAA666A00011A21)
Dodavatel: ERLAB CAPTAIRE
Popis: The new Captair® Smart ductless filtering hoods are designed with a simple and innovative way of communication. Smart Technology, simple and intuitive communication by light indicates the status of the hood.
Please complete the quote request to enable us to assist you in finding the right unit for your application.
https://cz.cmd2.vwr.com/bin/public/fc/main?f=Y5&pimid=18763661
Měrná jednotka: 1 * 1 KS

New Product


Cena na vyžádání
Omezené množství produktu na skladě. Zboží může být k dispozici v jiném skladě poblíž vašeho sídla. Přesvědčte se, že jste přihlášení na stránky, abyste mohli vidět dostupné položky na skladě. Pokud je stále zobrazeno call a potřebujete asistenci, volejte na číslo 321 570 321.
Omezené množství produktu na skladě. Zboží může být k dispozici v jiném skladě poblíž vašeho sídla. Přesvědčte se, že jste přihlášení na stránky, abyste mohli vidět dostupné položky na skladě. Pokud je stále zobrazeno call a potřebujete asistenci, volejte na číslo 321 570 321.
Daná chemikálie je regulována dle platné legislativy a bude vyžadováno vyplnění formuláře. Jeho včasným vyplněním uspíšíte dodání produktu.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Tento produkt je zablokován vaší organizací. Kontaktujte své nákupní oddělení pro více informací.
Původní produkt již není k dispozici. Zobrazen je náhradní produkt.
Tento produkt již není k dispozici. Podobné produkty můžete vyhledat pomocí VWR katalogových čísel nebo čísel dodavatele uvedených výše. Pokud potřebujete další asistenci, zavolejte na telefonní číslo zákaznického servisu VWR 321 570 321.
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