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Catalogus nummer: (USBI044799)
Leverancier: US Biological
Omschrijving: Anti-FGF-21 Mouse Monoclonal Antibody [clone: FG348-1]
UOM: 1 * 1 EA


Leverancier: VWR Collection
Omschrijving: Binder-free glass fibre filters feature fast flow rates, high loading capacity, wide thermal tolerance and excellent precipitate retention.

Leverancier: Thermo Fisher Scientific
Omschrijving: Aluminum, silver coated (19 - 21% Ag) (w/w) ≥99.9% (metals basis), powder -200 mesh
Leverancier: SWANN MORTON
Omschrijving: Met roestvrijstalen mesje en kunststof handvat.
Catalogus nummer: (ABCAAB214632-100)
Leverancier: Abcam
Omschrijving: Alexa Fluor® 488 Rabbit monoclonal [E121-21] to STAT3.
UOM: 1 * 100 µl


Leverancier: Abcam
Omschrijving: Rabbit monoclonal [EPR22877-21] to Nup107 - BSA and Azide free.

Catalogus nummer: (340374T)
Leverancier: VWR Chemicals
Omschrijving: Hematoxylin hydrate, Gurr™ for microscopical staining
UOM: 1 * 25 g

Catalogus nummer: (ABCAAB214939-100)
Leverancier: Abcam
Omschrijving: Alexa Fluor® 647 Rabbit monoclonal [E121-21] to STAT3.
UOM: 1 * 100 µl


Catalogus nummer: (USBIM4688-23A)
Leverancier: US Biological
Omschrijving: Anti-ABCC3 Mouse Monoclonal Antibody [clone: M3II-21]
UOM: 1 * 1 mL


Catalogus nummer: (ABCAAB18435-50)
Leverancier: Abcam
Omschrijving: FITC Mouse IgG1, kappa monoclonal [MOPC-21] - Isotype control.
UOM: 1 * 1 EA


Catalogus nummer: (ENZOBMLGR2330025)
Leverancier: ENZO LIFE SCIENCES
Omschrijving: Constitutive androstane receptor ligand.
UOM: 1 * 25 mg


Catalogus nummer: (BOSSBS-15126R-A750)
Leverancier: Bioss
Omschrijving: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C21orf59, also known as C21orf48, is a 290 amino acid protein and its gene product has been provisionally designated C21orf59 pending further characterization.
UOM: 1 * 100 µl


Catalogus nummer: (BOSSBS-15126R-CY3)
Leverancier: Bioss
Omschrijving: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C21orf59, also known as C21orf48, is a 290 amino acid protein and its gene product has been provisionally designated C21orf59 pending further characterization.
UOM: 1 * 100 µl


Catalogus nummer: (BOSSBS-15126R-CY5)
Leverancier: Bioss
Omschrijving: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C21orf59, also known as C21orf48, is a 290 amino acid protein and its gene product has been provisionally designated C21orf59 pending further characterization.
UOM: 1 * 100 µl


Catalogus nummer: (BOSSBS-15126R-FITC)
Leverancier: Bioss
Omschrijving: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C21orf59, also known as C21orf48, is a 290 amino acid protein and its gene product has been provisionally designated C21orf59 pending further characterization.
UOM: 1 * 100 µl


Catalogus nummer: (BOSSBS-15126R-CY7)
Leverancier: Bioss
Omschrijving: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C21orf59, also known as C21orf48, is a 290 amino acid protein and its gene product has been provisionally designated C21orf59 pending further characterization.
UOM: 1 * 100 µl


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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