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U heeft gezocht op: 2,3,5-Tribromo-4-methylthiophene


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Image Unavailable-EHERXA17883500ME

Organische referentiestandaard, 2,3,5-Trimethylphenol 100 µg/ml in methanol

Catalogus nummer: (EHERXA17883500ME)
Leverancier: EHRENSTORFER
Omschrijving: Organic Standard, 2,3,5-Trimethylphenol 100 µg/ml in methanol, Verpakking: Glass bottle
UOM: 1 * 1 mL
Image Unavailable-BOSSBS-13623R-CY5

Anti-TMEM176A Rabbit Polyclonal Antibody (Cy5®)

Catalogus nummer: (BOSSBS-13623R-CY5)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13623R-CY3

Anti-TMEM176A Rabbit Polyclonal Antibody (Cy3®)

Catalogus nummer: (BOSSBS-13623R-CY3)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image Unavailable-EHERL17773500IO

Pesticide referentiestandaard, 2,3,5-Trichloorfenol 10 µg/ml in iso-octaan

Catalogus nummer: (EHERL17773500IO)
Leverancier: EHRENSTORFER
Omschrijving: Organic Standard, 2,3,5-Trichloorfenol 10 µg/ml in iso-octaan, Verpakking: Glass bottle
UOM: 1 * 10 mL
Image Unavailable-BOSSBS-13623R-A647

Anti-TMEM176A Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalogus nummer: (BOSSBS-13623R-A647)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image Unavailable-EHERL17775200IO

Pesticide referentiestandaard, 2,3,5-Trichlorophenyl acetate 10 µg/ml in isooctane

Catalogus nummer: (EHERL17775200IO)
Leverancier: EHRENSTORFER
Omschrijving: Organic Standard, 2,3,5-Trichlorophenyl acetate 10 µg/ml in isooctane, Verpakking: Glass bottle
UOM: 1 * 10 mL
Image Unavailable-ANTIA316504-100

Anti-Human Nuclear Antigen Rabbit Recombinant Antibody [clone: 235-1R]

Catalogus nummer: (ANTIA316504-100)
Leverancier: ANTIBODIES.COM
Omschrijving: Recombinant rabbit monoclonal [235-1R] antibody to human Nuclear Antigen for IHC-P with samples derived from human.
UOM: 1 * 1 EA

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Image Unavailable-ANTIA315120-100

Anti-Human Nuclear Antigen Rabbit Recombinant Antibody [clone: 235-1R]

Catalogus nummer: (ANTIA315120-100)
Leverancier: ANTIBODIES.COM
Omschrijving: Recombinant rabbit monoclonal [235-1R] antibody to human Nuclear Antigen for IHC-P with samples derived from human.
UOM: 1 * 1 EA

New Product


Image Unavailable-PROOCIL-PCB-23

Organische referentiestandaard, 2,3,5-Trichlorobiphenyl (PCB No. 23) 35 µg/ml in isooctane

Catalogus nummer: (PROOCIL-PCB-23)
Leverancier: LGC Standards PROMOCHEM
Omschrijving: Organic Standard, 2,3,5-Trichlorobiphenyl (PCB No. 23) 35 µg/ml in isooctane, Verpakking: Glass bottle
UOM: 1 * 1 mL
Product Image-223-1151

Threaded fittings

Catalogus nummer: (223-1151)
Leverancier: BURKLE
Omschrijving: Nipple, with outer thread, NW 23,5 mm, PP, Schroefdraad: 25,4 mm
UOM: 1 * 1 ST
Image Unavailable-AESCFL437R

Gouges, Aesculap®

Leverancier: Aesculap
Omschrijving: Aesculap®, Lamina gouge, cranked, Type: Capener, Breedte: 8 mm, Lengte: 235 mm

Image Unavailable-ANTIA250966-100

Anti-Nuclear Antigen Mouse Monoclonal Antibody [clone: 235-1]

Catalogus nummer: (ANTIA250966-100)
Leverancier: ANTIBODIES.COM
Omschrijving: Anti-Nuclear Antigen Mouse Monoclonal Antibody [clone: 235-1]
UOM: 1 * 1 EA

New Product


Image Unavailable-AESCJF166

Filter papers with or without process indicator, Aesculap®

Catalogus nummer: (AESCJF166)
Leverancier: Aesculap
Omschrijving: Filterpapier, kwalitatief, Aesculap®, With process indicator, 118×235 mm
UOM: 1 * 100 ST
Image Unavailable-BOSSBS-13623R

Anti-TMEM176A Rabbit Polyclonal Antibody

Catalogus nummer: (BOSSBS-13623R)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13623R-A350

Anti-TMEM176A Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Catalogus nummer: (BOSSBS-13623R-A350)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Product Image-ANTIA254146-100

Anti-Human Nuclear Antigen Mouse Monoclonal Antibody [Clone: 235-1]

Catalogus nummer: (ANTIA254146-100)
Leverancier: ANTIBODIES.COM
Omschrijving: Mouse monoclonal [235-1] antibody to human Nuclear Antigen for Flow Cytometry, IF, IP, ICC and IHC-Fr with samples derived from human and Non-Human Primates.
UOM: 1 * 1 EA

New Product


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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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