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Supplier: Merck
Description: Potassium formate, Sigma-Aldrich®

Catalog Number: (BOSSBS-13138R-CY5)
Supplier: Bioss
Description: Fanconi anemia (FA) is an autosomal recessive disorder characterized by bone marrow failure, birth defects and chromosomal instability. At the cellular level, FA is characterized by spontaneous chromosomal breakage and a unique hypersensitivity to DNA cross-linking agents. At least eight complementation groups (A-G) have been identified and six FA genes (for subtypes A, C, D2, E, F and G) have been cloned. The FA proteins lack sequence homologies or motifs that could point to a molecular function. The cellular accumulation of FA proteins, including FANCA and FANCG, is subject to regulation by TNF alpha signaling. Phosphorylation of FANC (Fanconi anemia complementation group) proteins is thought to be important for the function of the FA pathway. FANCA, also known as FACA and FANCH, associates with the Brm-related gene 1 (BRG1) product, a subunit of the SWI/SNF complex which remodels chromatin structure through a DNA-dependent ATPase activity. FANCA is mainly expressed in lymphoid tissues, testis and ovary. The amino-terminal region of the FANCA protein is required for FANCG binding, FANCC binding, nuclear localization and functional activity of the complex. The human FANCA gene maps to chromosome 16q24.3 and encodes a 1,455 amino acid protein.
UOM: 1 * 100 µl


Catalog Number: (SIAL03951-50ML)
Supplier: Merck
Description: N-Ethylformamide, Sigma-Aldrich®
UOM: 1 * 50 mL


Catalog Number: (BOSSBS-13138R-A680)
Supplier: Bioss
Description: Fanconi anemia (FA) is an autosomal recessive disorder characterized by bone marrow failure, birth defects and chromosomal instability. At the cellular level, FA is characterized by spontaneous chromosomal breakage and a unique hypersensitivity to DNA cross-linking agents. At least eight complementation groups (A-G) have been identified and six FA genes (for subtypes A, C, D2, E, F and G) have been cloned. The FA proteins lack sequence homologies or motifs that could point to a molecular function. The cellular accumulation of FA proteins, including FANCA and FANCG, is subject to regulation by TNF alpha signaling. Phosphorylation of FANC (Fanconi anemia complementation group) proteins is thought to be important for the function of the FA pathway. FANCA, also known as FACA and FANCH, associates with the Brm-related gene 1 (BRG1) product, a subunit of the SWI/SNF complex which remodels chromatin structure through a DNA-dependent ATPase activity. FANCA is mainly expressed in lymphoid tissues, testis and ovary. The amino-terminal region of the FANCA protein is required for FANCG binding, FANCC binding, nuclear localization and functional activity of the complex. The human FANCA gene maps to chromosome 16q24.3 and encodes a 1,455 amino acid protein.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-13138R-HRP)
Supplier: Bioss
Description: Fanconi anemia (FA) is an autosomal recessive disorder characterized by bone marrow failure, birth defects and chromosomal instability. At the cellular level, FA is characterized by spontaneous chromosomal breakage and a unique hypersensitivity to DNA cross-linking agents. At least eight complementation groups (A-G) have been identified and six FA genes (for subtypes A, C, D2, E, F and G) have been cloned. The FA proteins lack sequence homologies or motifs that could point to a molecular function. The cellular accumulation of FA proteins, including FANCA and FANCG, is subject to regulation by TNF alpha signaling. Phosphorylation of FANC (Fanconi anemia complementation group) proteins is thought to be important for the function of the FA pathway. FANCA, also known as FACA and FANCH, associates with the Brm-related gene 1 (BRG1) product, a subunit of the SWI/SNF complex which remodels chromatin structure through a DNA-dependent ATPase activity. FANCA is mainly expressed in lymphoid tissues, testis and ovary. The amino-terminal region of the FANCA protein is required for FANCG binding, FANCC binding, nuclear localization and functional activity of the complex. The human FANCA gene maps to chromosome 16q24.3 and encodes a 1,455 amino acid protein.
UOM: 1 * 100 µl


Supplier: Thermo Fisher Scientific
Description: N,N-Dimethylformamide 99.5% for HPLC
Supplier: Thermo Fisher Scientific
Description: N,N-Dimethylformamide, extra dry over Molecular Sieve 99.8%, AcroSeal®
Supplier: Merck
Description: Benzyl formate, Sigma-Aldrich®

Supplier: Merck
Description: Ethyl formate, Sigma-Aldrich®

Supplier: Thermo Fisher Scientific
Description: N,N-Dimethylformamide ≥99%
Catalog Number: (SIAL433764-25G)
Supplier: Merck
Description: Cesium formate, Sigma-Aldrich®
UOM: 1 * 25 g


Supplier: Thermo Fisher Scientific
Description: Ammonium formate 99%
Supplier: Thermo Fisher Scientific
Description: N,N-Dimethylformamide 99+%, extra pure
Catalog Number: (SIALW294306-4KG-K)
Supplier: Merck
Description: Propyl formate, Sigma-Aldrich®
UOM: 1 * 4 kg


Catalog Number: (SIAL245852-100ML)
Supplier: Merck
Description: Propyl formate, Sigma-Aldrich®
UOM: 1 * 100 mL


Catalog Number: (EHERC13913300)
Supplier: EHRENSTORFER
Description: Butyl formate
UOM: 1 * 0,25 g


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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.
Dual use goods can only be delivered within the European Union.
Dual use goods can only be delivered within the European Union.
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