Sie suchten nach: Pyridoxal+Hydrochlorid

Artikel-Nr: (BOSSBS-9027R-CY3)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-9027R-CY3

Beschreibung: This gene encodes a long chain base subunit of serine palmitoyltransferase. Serine palmitoyltransferase, which consists of two different subunits, is the key enzyme in sphingolipid biosynthesis. It catalyzes the pyridoxal-5-prime-phosphate-dependent condensation of L-serine and palmitoyl-CoA to 3-oxosphinganine. Mutations in this gene were identified in patients with hereditary sensory neuropathy type I. [provided by RefSeq, Mar 2011].

UOM: 1 * 100 µl

Sale

Artikel-Nr: (AVIVARP43518T10025)

Lieferant: Aviva Systems Biology

Hersteller Artikel Nummer : ARP43518T10025

Beschreibung: Glutamic-oxaloacetic transaminase is a pyridoxal phosphate-dependent enzyme which exists in cytoplasmic and inner-membrane mitochondrial forms, GOT1 and GOT2, respectively. GOT plays a role in amino acid metabolism and the urea and tricarboxylic acid cycles. The two enzymes are homodimeric and show close homology.

UOM: 1 * 25 µl

Sale

Artikel-Nr: (BOSSBS-9027R-A350)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-9027R-A350

Beschreibung: This gene encodes a long chain base subunit of serine palmitoyltransferase. Serine palmitoyltransferase, which consists of two different subunits, is the key enzyme in sphingolipid biosynthesis. It catalyzes the pyridoxal-5-prime-phosphate-dependent condensation of L-serine and palmitoyl-CoA to 3-oxosphinganine. Mutations in this gene were identified in patients with hereditary sensory neuropathy type I. [provided by RefSeq, Mar 2011].

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-9027R-A488)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-9027R-A488

Beschreibung: This gene encodes a long chain base subunit of serine palmitoyltransferase. Serine palmitoyltransferase, which consists of two different subunits, is the key enzyme in sphingolipid biosynthesis. It catalyzes the pyridoxal-5-prime-phosphate-dependent condensation of L-serine and palmitoyl-CoA to 3-oxosphinganine. Mutations in this gene were identified in patients with hereditary sensory neuropathy type I. [provided by RefSeq, Mar 2011].

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-9027R-A555)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-9027R-A555

Beschreibung: This gene encodes a long chain base subunit of serine palmitoyltransferase. Serine palmitoyltransferase, which consists of two different subunits, is the key enzyme in sphingolipid biosynthesis. It catalyzes the pyridoxal-5-prime-phosphate-dependent condensation of L-serine and palmitoyl-CoA to 3-oxosphinganine. Mutations in this gene were identified in patients with hereditary sensory neuropathy type I. [provided by RefSeq, Mar 2011].

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-9027R-FITC)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-9027R-FITC

Beschreibung: This gene encodes a long chain base subunit of serine palmitoyltransferase. Serine palmitoyltransferase, which consists of two different subunits, is the key enzyme in sphingolipid biosynthesis. It catalyzes the pyridoxal-5-prime-phosphate-dependent condensation of L-serine and palmitoyl-CoA to 3-oxosphinganine. Mutations in this gene were identified in patients with hereditary sensory neuropathy type I. [provided by RefSeq, Mar 2011].

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-4143R-A647)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-4143R-A647

Beschreibung: This enzyme has 2 functions: it catalyzes the production of glutamine and 4-aminobutanoate (gamma-aminobutyric acid, GABA), the latter in a pyridoxal phosphate-independent manner (By similarity). Essential for proliferation of fetal skin fibroblasts.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-4143R-A750)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-4143R-A750

Beschreibung: This enzyme has 2 functions: it catalyses the production of glutamine and 4-aminobutanoate (gamma-aminobutyric acid, GABA), the latter in a pyridoxal phosphate-independent manner (By similarity). Essential for proliferation of foetal skin fibroblasts.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-4143R-HRP)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-4143R-HRP

Beschreibung: This enzyme has 2 functions: it catalyzes the production of glutamine and 4-aminobutanoate (gamma-aminobutyric acid, GABA), the latter in a pyridoxal phosphate-independent manner (By similarity). Essential for proliferation of fetal skin fibroblasts.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-11822R-A350)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-11822R-A350

Beschreibung: CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-13494R-FITC)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13494R-FITC

Beschreibung: GOT1L1, Glutamate oxaloacetate transaminase 1-like protein 1, is a 421 amino acid member of the class-I pyridoxal-phosphate-dependent aminotransferase family. Similar to glutamate-oxaloacetate transaminase (GOT1), GOT1L1 is found primarily as a homodimer in the cytoplasmic space but also has mitochondrial and chloroplastic isozymes. GOT1L1 transaminates 2-oxoglutarate with L-aspartate to yield oxaloacetate and L-glutamate. This reaction requires a pyridoxal phosphate cofactor to occur. The GOT1L1 peptidase is predominately expressed in the liver and serum levels of this protein can be used as an indicator of liver disease. Also, elevated glutamate concentrations in the brain interstitial fluids can lead to pathological brain conditions. The glutamate-scavenging properties of these aminotranferase type enzymes likely prevent glutamate excitotoxicity and the long-lasting neurological deficits seen after stroke.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-9027R-CY7)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-9027R-CY7

Beschreibung: This gene encodes a long chain base subunit of serine palmitoyltransferase. Serine palmitoyltransferase, which consists of two different subunits, is the key enzyme in sphingolipid biosynthesis. It catalyzes the pyridoxal-5-prime-phosphate-dependent condensation of L-serine and palmitoyl-CoA to 3-oxosphinganine. Mutations in this gene were identified in patients with hereditary sensory neuropathy type I. [provided by RefSeq, Mar 2011].

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-11822R-CY5)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-11822R-CY5

Beschreibung: CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-13370R-A350)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13370R-A350

Beschreibung: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-13370R-CY5)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13370R-CY5

Beschreibung: The glycine cleavage system is comprised of AMT (known as Protein T), GCSH (known as Protein H), DLD (known as Protein L) and GLDC (known as Protein P), all of which work together to catalyze the cleavage and degradation of glycine. GLDC (glycine dehydrogenase ), also known as GCE, GCSP (glycine cleavage system P protein) or HYGN1, is a 1,020 amino acid protein that localizes to the mitochondria and belongs to the gcvP family. GLDC binds to glycine and enables the methylamine group from glycine to be transferred to the Protein T. GLDC exists as a homodimer and utilizes pyridoxal phosphate as a cofactor. Mutations in the gene encoding GLDC leads to nonketotic hyperglycinemia (NKH), also known as glycine encephalopathy (GCE), an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-11822R-A680)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-11822R-A680

Beschreibung: CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyses the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

UOM: 1 * 100 µl

Sale