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Image Unavailable-BWRLBS2737

Anti-NMBR Rabbit Polyclonal Antibody [clone: L264]

Catalog Number: (BWRLBS2737)
Supplier: Bioworld Technology
Description: Synthetic peptide, corresponding to amino acids 235-280 of Human NMBR.
UOM: 1 * 100 µG
Image Unavailable-BOSSBS-13623R-CY5

Anti-TMEM176A Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-13623R-CY5)
Supplier: Bioss
Description: 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®)

Catalog Number: (BOSSBS-13623R-CY3)
Supplier: Bioss
Description: 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)

Catalog Number: (BOSSBS-13623R-A555)
Supplier: Bioss
Description: 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-CY7

Anti-TMEM176A Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-13623R-CY7)
Supplier: Bioss
Description: 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)

Catalog Number: (BOSSBS-13623R-A488)
Supplier: Bioss
Description: 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))

Catalog Number: (BOSSBS-13623R-HRP)
Supplier: Bioss
Description: 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-FITC

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

Catalog Number: (BOSSBS-13623R-FITC)
Supplier: Bioss
Description: 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)

Catalog Number: (BOSSBS-13623R-A647)
Supplier: Bioss
Description: 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

Catalog Number: (BOSSBS-13623R)
Supplier: Bioss
Description: 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)

Catalog Number: (BOSSBS-13623R-A350)
Supplier: Bioss
Description: 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-SIAL357782-1G

2,3,5-Trichlorobenzoic acid, Sigma-Aldrich®

Catalog Number: (SIAL357782-1G)
Supplier: Merck
Description: 2,3,5-Trichlorobenzoic acid, Sigma-Aldrich®
UOM: 1 * 1 g
Image Unavailable-T8877-25G

2,3,5-Triphenyltetrazolium chloride (TTC) ≥98% (by HPLC), Sigma-Aldrich®

Supplier: SIGMA ALDRICH MICROSCOPY
Description: 2,3,5-Triphenyltetrazolium chloride (TTC) ≥98% (by HPLC), Sigma-Aldrich®

Certificates

Product Image-28804.121

2,3,5-Triphenyltetrazolium chloride (TTC), TECHNICAL

Catalog Number: (28804.121)
Supplier: VWR Chemicals
Description: 2,3,5-Triphenyltetrazolium chloride (TTC), TECHNICAL
UOM: 1 * 10 g

MSDS Certificates


Image Unavailable-ICNA0219519910

Glutaraldehyde 25% in aqueous solution

Supplier: MP Biomedicals
Description: 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.

Image Unavailable-APOSPC303012-5G

2,3,5-Trifluorobenzylamine 97%

Supplier: Apollo Scientific
Description: 2,3,5-Trifluorobenzylamine 97%

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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 +43 1 97002 - 0.
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 +43 1 97002 - 0.
Dual use goods can only be delivered within the European Union.
Dual use goods can only be delivered within the European Union.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
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