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Image non disponible-APOSPC7775-100G

Ethyl-2,3,4-trifluorobenzoate

Fournisseur: Apollo Scientific
Description: Ethyl-2,3,4-trifluorobenzoate

Image non disponible-APOSPC7793-100G

Ethyl-2,4,5-trifluorobenzoate

Fournisseur: Apollo Scientific
Description: Ethyl-2,4,5-trifluorobenzoate

Image non disponible-APOSPC300696-100G

Methyl 2,4,5-trifluorobenzoate 99%

Fournisseur: Apollo Scientific
Description: Methyl 2,4,5-trifluorobenzoate 99%

Image non disponible-APOSPC51486-1G

Methyl 6-bromo-2,3,4-trifluorobenzoate

Fournisseur: Apollo Scientific
Description: Methyl 6-bromo-2,3,4-trifluorobenzoate

Image non disponible-APOSPC502386-1G

Methyl 3-bromo-2,4,5-trifluorobenzoate 95+%

Fournisseur: Apollo Scientific
Description: Methyl 3-bromo-2,4,5-trifluorobenzoate 95+%

Image non disponible-APOSPC48003-1G

Methyl 5-bromo-2,3,4-trifluorobenzoate 95%

Fournisseur: Apollo Scientific
Description: Methyl 5-bromo-2,3,4-trifluorobenzoate 95%

Image non disponible-BWRLBS3796

Anti-ACAT1 Rabbit Polyclonal Antibody [clone: K266]

Numéro de catalogue: (BWRLBS3796)
Fournisseur: Bioworld Technology
Description: Synthetic peptide, corresponding to amino acids 235-286 of Human ACAT1.
UOM: 1 * 1 EA
Image non disponible-APOSPC50435-100G

Methyl-2,4,6-trifluorobenzoate 98%

Fournisseur: Apollo Scientific
Description: Methyl-2,4,6-trifluorobenzoate 98%

Image non disponible-BWRLBS2737

Anti-NMBR Rabbit Polyclonal Antibody [clone: L264]

Numéro de catalogue: (BWRLBS2737)
Fournisseur: Bioworld Technology
Description: Synthetic peptide, corresponding to amino acids 235-280 of Human NMBR.
UOM: 1 * 1 EA
Image non disponible-APOSPC48810-5G

Methyl 4-bromo-2,3,6-trifluorobenzoate 95%

Fournisseur: Apollo Scientific
Description: Methyl 4-bromo-2,3,6-trifluorobenzoate 95%

Image non disponible-APOSPC53605-5G

Methyl 3-chloro-2,4,5-trifluorobenzoate ≥95%

Fournisseur: Apollo Scientific
Description: Methyl 3-chloro-2,4,5-trifluorobenzoate ≥95%

Image non disponible-BOSSBS-13623R-CY5

Anti-TMEM176A Rabbit Polyclonal Antibody (Cy5®)

Numéro de catalogue: (BOSSBS-13623R-CY5)
Fournisseur: 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 non disponible-BOSSBS-13623R-CY3

Anti-TMEM176A Rabbit Polyclonal Antibody (Cy3®)

Numéro de catalogue: (BOSSBS-13623R-CY3)
Fournisseur: 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 non disponible-BOSSBS-13623R-HRP

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

Numéro de catalogue: (BOSSBS-13623R-HRP)
Fournisseur: 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 non disponible-BOSSBS-13623R-FITC

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

Numéro de catalogue: (BOSSBS-13623R-FITC)
Fournisseur: 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 non disponible-BOSSBS-13623R-A488

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

Numéro de catalogue: (BOSSBS-13623R-A488)
Fournisseur: 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
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