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Image Unavailable-BOSSBS-13623R-CY7

Anti-TMEM176A Rabbit Polyclonal Antibody (Cy7®)

Artikel-Nr: (BOSSBS-13623R-CY7)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-13623R-CY7
Beschreibung: 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-A555

Anti-TMEM176A Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Artikel-Nr: (BOSSBS-13623R-A555)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-13623R-A555
Beschreibung: 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

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Image Unavailable-BOSSBS-13623R-FITC

Anti-TMEM176A Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Artikel-Nr: (BOSSBS-13623R-FITC)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-13623R-FITC
Beschreibung: 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-HRP

Anti-TMEM176A Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Artikel-Nr: (BOSSBS-13623R-HRP)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-13623R-HRP
Beschreibung: 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-A488

Anti-TMEM176A Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Artikel-Nr: (BOSSBS-13623R-A488)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-13623R-A488
Beschreibung: 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-A647

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

Artikel-Nr: (BOSSBS-13623R-A647)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-13623R-A647
Beschreibung: 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

Anti-TMEM176A Rabbit Polyclonal Antibody

Artikel-Nr: (BOSSBS-13623R)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-13623R
Beschreibung: 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)

Artikel-Nr: (BOSSBS-13623R-A350)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-13623R-A350
Beschreibung: 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-CY5

Anti-TMEM176A Rabbit Polyclonal Antibody (Cy5®)

Artikel-Nr: (BOSSBS-13623R-CY5)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-13623R-CY5
Beschreibung: 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®)

Artikel-Nr: (BOSSBS-13623R-CY3)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-13623R-CY3
Beschreibung: 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-APOSPC10372-1G

Methyl-3,4,5-trifluorobenzenecarboxylate 99%

Lieferant: Apollo Scientific
Beschreibung: Methyl-3,4,5-trifluorobenzenecarboxylate 99%

Image Unavailable-EHERC17870000

2,3,5-Triiodbenzoesäure

Artikel-Nr: (EHERC17870000)
Lieferant: EHRENSTORFER
Hersteller Artikel Nummer : C17870000
Beschreibung: 2,3,5-Triiodbenzoesäure
UOM: 1 * 0,25 g
Image Unavailable-ACTIAS23123G1

2,3,5-Trifluor-4-methylbenzoesäure

Lieferant: ACTIVATE SCIENTIFIC
Beschreibung: 2,3,5-Trifluor-4-methylbenzoesäure

Image Unavailable-T8877-50G

2,3,5-Triphenyltetrazoliumchlorid ≥98% (durch HPLC), Sigma-Aldrich®

Lieferant: SIGMA ALDRICH MICROSCOPY
Beschreibung: 2,3,5-Triphenyltetrazoliumchlorid ≥98% (durch HPLC), Sigma-Aldrich®

Product Image-28804.121

2,3,5-Triphenyltetrazoliumchlorid, TECHNICAL

Artikel-Nr: (28804.121)
Lieferant: VWR Chemicals
Beschreibung: 2,3,5-Triphenyltetrazoliumchlorid, TECHNICAL
UOM: 1 * 10 g

Sicherheitsdatenblätter Zertifikate


Image Unavailable-ICNA0219519980

Glutaraldehyd 25% in wässriger Lösung

Lieferant: MP Biomedicals
Beschreibung: Glutaraldehyde is also referred to as glutaral, 1,5-pentanedione, potentiated acid glutaraldehyde, sonacide, and glutardialdehyde. Pure monomeric glutaraldehyde has an absorbance peak at 280 nm and the main impurity, possibly a polymer, has an absorbance peak at 235 nm. Upon analysis, this product is 25-28% by titration and has an A235/A280 ratio of not more than 0,5. Monomeric glutaraldehyde may be purified from polymeric glutaraldehyde by treatment with charcoal (5% w/v) and subsequent filtration (3-4 times). Untreated glutaraldehyde has an absorption at 235 nm that is 5 times greater than that at 280 nm, whereas, after three washings the values are about equal. Glutaraldehyde is a bifunctional cross-linking reagent, reacting with NH2 groups to form Schiff's bases.

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Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das call noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 044 745 13 13.
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