Esta buscando: N-Acetyl-L-glutamic+acid


106 671  results were found

SearchResultCount:"106671"

Sort Results

Vista lista Vista Extendida (Nueva)

Valore los resultados de su búsqueda

Numero del catalogo: (BOSSBS-8499R-A488)
Proveedor: Bioss
Descripción: The function of RED is currently unknown. The protein encoded by the RED gene was identified by its RED repeat, a stretch of repeated arginine, glutamic acid and aspartic acid residues. The protein localizes to discrete dots within the nucleus, excluding the nucleolus. This gene maps to chromosome 5; however, a pseudogene may exist on chromosome 2.
UOM: 1 * 100 µl


Proveedor: Apollo Scientific
Descripción: 3-Acetyl-2-pyridine carboxylic acid

Nueva transparencia para los clientes europeos

¿Ha observado nuestra nueva visibilidad mejorada de la ubicación del stock en el paso de adquisición?

Más información

Mejora para las ubicaciones de stock

Numero del catalogo: (BOSSBS-8499R-CY7)
Proveedor: Bioss
Descripción: The function of RED is currently unknown. The protein encoded by the RED gene was identified by its RED repeat, a stretch of repeated arginine, glutamic acid and aspartic acid residues. The protein localizes to discrete dots within the nucleus, excluding the nucleolus. This gene maps to chromosome 5; however, a pseudogene may exist on chromosome 2.
UOM: 1 * 100 µl


Numero del catalogo: (BOSSBS-8499R-CY5)
Proveedor: Bioss
Descripción: The function of RED is currently unknown. The protein encoded by the RED gene was identified by its RED repeat, a stretch of repeated arginine, glutamic acid and aspartic acid residues. The protein localizes to discrete dots within the nucleus, excluding the nucleolus. This gene maps to chromosome 5; however, a pseudogene may exist on chromosome 2.
UOM: 1 * 100 µl


Numero del catalogo: (TCIAA2555-5G)
Proveedor: TCI
Descripción: 5-Acetyl-1,3-dimethylbarbituric acid 98,0 GC, T
UOM: 1 * 5 g


Numero del catalogo: (APOSBIA1219-25G)
Proveedor: Apollo Scientific
Descripción: N-Acetyl-L-alanine
UOM: 1 * 25 g


Numero del catalogo: (BOSSBS-8403R-CY5)
Proveedor: Bioss
Descripción: Glutamate receptors mediate most excitatory neurotransmission in the brain and play an important role in neural plasticity, neural development and neurodegeneration. Ionotropic glutamate receptors are categorized into NMDA receptors and kainate/AMPA receptors, both of which contain glutamate-gated, cation-specific ion channels. Synaptic and extrasynaptic NMDA receptors have been shown to have opposite effects on neuronal survival, CREB function and gene regulation. Gcom1 (GRINL1A complex locus protein 1), also known as GUP (GRINL1A upstream protein) and Gcom (GRINL1A combined protein), is a 466 amino acid protein that is a component of the GRINL1A complex transcription unit, which is thought to be involved in the modulation of glutamatergic neurotransmission through interaction with the NR1 subunit of the NMDA receptor. Gcom1 is expressed in small intestine, lung, liver, heart, skeletal muscle, testis and prostate and also colocalizes with NR1 in cortical and hippocampal neurons. There are eleven isoforms of Gcom1 that are produced as a result of alternative splicing events.
UOM: 1 * 100 µl


Numero del catalogo: (BOSSBS-11381R-A680)
Proveedor: Bioss
Descripción: Contributes to degradation of proteins cross-linked by transglutaminases. Degrades the cross-link between a lysine and a glutamic acid residue from two proteins that have been cross-linked by transglutaminases. catalyses the formation of 5-oxoproline from L-gamma-glutamyl-L-epsilon-lysine. Inactive with L-gamma-glutamyl-alpha-amino acid substrates such as L-gamma-glutamyl-L-alpha-cysteine and L-gamma-glutamyl-L-alpha-alanine.
UOM: 1 * 100 µl


Numero del catalogo: (BOSSBS-13390R-A680)
Proveedor: Bioss
Descripción: GLUD2 is both mitochondrial matrix enzymes belonging to the Glu/Leu/Phe/Val dehydrogenases family. Exisiting as homohexamers, GLUD1 catalyzes the oxidative deamination of glutamate to ?ketoglutarate and ammonia while GLUD2 is involved in the recycling of glutamate during neurotransmission. GLUD1 is critical for regulating amino acid induced insulin secretion and is allosterically activated by ADP and inhibited by GTP and ATP. Mutations in the gene encoding GLUD1 causes hyperinsulinism-hyperammonemia syndrome (HHS), which is an inherited condition characterized by high insulin and ammonia levels in the blood. GLUD1 may also be involved in learning and memory reactions by increasing the turnover of the excitatory neurotransmitter glutamate. GLUD2 is expressed in testis and retina, with lower levels found in brain.
UOM: 1 * 100 µl


Proveedor: Apollo Scientific
Descripción: 2,3,5-Tri-O-acetyl-D-xylonic acid, γ-lactone ≥98%

Numero del catalogo: (APOSOR451038-5G)
Proveedor: Apollo Scientific
Descripción: 1-Acetyl-3-azetidinecarboxylic acid methyl ester
UOM: 1 * 5 g


Numero del catalogo: (APOSOR913438-1G)
Proveedor: Apollo Scientific
Descripción: (2-Acetyl-phenoxy)-acetic acid 95%
UOM: 1 * 1 g


Numero del catalogo: (BOSSBS-8499R-A680)
Proveedor: Bioss
Descripción: The function of RED is currently unknown. The protein encoded by the RED gene was identified by its RED repeat, a stretch of repeated arginine, glutamic acid and aspartic acid residues. The protein localises to discrete dots within the nucleus, excluding the nucleolus. This gene maps to chromosome 5; however, a pseudogene may exist on chromosome 2.
UOM: 1 * 100 µl


Proveedor: Thermo Fisher Scientific
Descripción: N-Acetyl-L-alanine 96%
Numero del catalogo: (BOSSBS-8499R-HRP)
Proveedor: Bioss
Descripción: The function of RED is currently unknown. The protein encoded by the RED gene was identified by its RED repeat, a stretch of repeated arginine, glutamic acid and aspartic acid residues. The protein localizes to discrete dots within the nucleus, excluding the nucleolus. This gene maps to chromosome 5; however, a pseudogene may exist on chromosome 2.
UOM: 1 * 100 µl


Numero del catalogo: (BOSSBS-8499R-A647)
Proveedor: Bioss
Descripción: The function of RED is currently unknown. The protein encoded by the RED gene was identified by its RED repeat, a stretch of repeated arginine, glutamic acid and aspartic acid residues. The protein localizes to discrete dots within the nucleus, excluding the nucleolus. This gene maps to chromosome 5; however, a pseudogene may exist on chromosome 2.
UOM: 1 * 100 µl


Consulta de precio
El stock para este material es limitada pero puede estar disponible en un almacén cerca de usted. Por favor, asegúrese de que ha iniciado sesión en la web para que el stock disponible se puede mostrar. Si el call sigue apareciendo y usted necesita ayuda, por favor llámenos al 902 222 897 o por email en webshop.es@avantorsciences.com.
El stock para este material es limitada pero puede estar disponible en un almacén cerca de usted. Por favor, asegúrese de que ha iniciado sesión en la web para que el stock disponible se puede mostrar. Si el call sigue apareciendo y usted necesita ayuda, por favor llámenos al 902 222 897 o por email en webshop.es@avantorsciences.com.
Este producto se trata de un artículo regulado sometido a normativa que restringe su venta. Si procede, nos pondremos en contacto con usted para solicitarle la licencia o declaración de uso necesaria para poder proceder al suministro del producto.
Este producto se trata de un artículo regulado sometido a normativa que restringe su venta.
Si procede, nos pondremos en contacto con usted para solicitarle la licencia o declaración de uso necesaria para poder proceder al suministro del producto.
Este producto ha sido bloqueado por su organización. Por favor, pónganse en contacto con su departamento de compras para obtener más información.
El producto original ya no está disponible. Su sustituto se muestra a continuación.
El producto(s) marcados con este símbolo están descatalogados - se venden hasta acabar stock. Pueden encontrar alternativas buscando con el número de catálogo VWR listado arriba. Si necesita más ayuda, por favor llame al Servicio de atención al cliente de VWR al 902.222.897.
305 - 320 of 106 671
no targeter for Bottom