cis-6-Amino-cyclohex-3-enecarboxylic+acid
Artikel-Nr:
(BOSSBS-6170R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6170R-A555
Lokale Artikelnummer::
BOSSBS-6170R-A555
Beschreibung:
RALA, resorcylic acid lactone alpha, is a low molecular weight GTP binding protein belonging to the RAS family of onco proteins. RALA has a 50% amino acid homology with RAS and an 85% homology with RALB. GTP binding proteins mediate the transmembrane signaling initiated by the occupancy of certain cell surface receptors.
VE:
1 * 100 µl
Artikel-Nr:
(32068.603)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC32068.603
Beschreibung:
EDTA Dinatriumsalz Konzentrat zur Verdünnung zu 0.01 mol in wässriger Lösung, ConvoL NORMADOSE® volumetrische Lösung
VE:
1 * 60 mL
Artikel-Nr:
(BOSSBS-5015R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5015R-A680
Lokale Artikelnummer::
BOSSBS-5015R-A680
Beschreibung:
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyse the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10150R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10150R-A750
Lokale Artikelnummer::
BOSSBS-10150R-A750
Beschreibung:
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyse the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13655R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13655R-A350
Lokale Artikelnummer::
BOSSBS-13655R-A350
Beschreibung:
Muskelin is a 735 amino acid nuclear and cytoplasmic protein that mediates cytoskeletal responses and cell spreading to Thrombospondin 1, an extracellular matrix glycoprotein. Forming a CTLH complex with RMND5A, Ran BP-M and TWA1, Muskelin exists as two alternatively spliced isoforms. Muskelin is implicated as an isoform-specific anchoring protein for the prostaglandin EP3 receptor, and contains one LisH domain, a CTLH domain, six Kelch repeats and an N-terminal discoidin-like domain through which it self-associates via a head-to-tail mechanism. Human and mouse Muskelin share 98% amino acid seqeuence homology and are encoded by genes located on chromosomes 7q32.3 and 6 A3.3, respectively.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5349R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5349R-A350
Lokale Artikelnummer::
BOSSBS-5349R-A350
Beschreibung:
PLM (FXYD1)is a member of a family of small membrane proteins that share a 35-amino acid signature sequence domain, beginning with the sequence PFXYD and containing 7 invariant and 6 highly conserved amino acids. FXYD2, also known as the gamma subunit of the Na,K-ATPase, regulates the properties of that enzyme. FXYD1 (phospholemman), FXYD2 (gamma), FXYD3 (MAT-8), FXYD4 (CHIF), and FXYD5 (RIC) have been shown to induce channel activity in experimental expression systems. PLM may be phosphorylated by several kinases, including protein kinase A, protein kinase C, NIMA kinase, and myotonic dystrophy kinase. It is thought to form an ion channel or regulate ion channel activity.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4104R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4104R-FITC
Lokale Artikelnummer::
BOSSBS-4104R-FITC
Beschreibung:
PLM (FXYD1)is a member of a family of small membrane proteins that share a 35-amino acid signature sequence domain, beginning with the sequence PFXYD and containing 7 invariant and 6 highly conserved amino acids. FXYD2, also known as the gamma subunit of the Na,K-ATPase, regulates the properties of that enzyme. FXYD1 (phospholemman), FXYD2 (gamma), FXYD3 (MAT-8), FXYD4 (CHIF), and FXYD5 (RIC) have been shown to induce channel activity in experimental expression systems. PLM may be phosphorylated by several kinases, including protein kinase A, protein kinase C, NIMA kinase, and myotonic dystrophy kinase. It is thought to form an ion channel or regulate ion channel activity.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13655R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13655R-A555
Lokale Artikelnummer::
BOSSBS-13655R-A555
Beschreibung:
Muskelin is a 735 amino acid nuclear and cytoplasmic protein that mediates cytoskeletal responses and cell spreading to Thrombospondin 1, an extracellular matrix glycoprotein. Forming a CTLH complex with RMND5A, Ran BP-M and TWA1, Muskelin exists as two alternatively spliced isoforms. Muskelin is implicated as an isoform-specific anchoring protein for the prostaglandin EP3 receptor, and contains one LisH domain, a CTLH domain, six Kelch repeats and an N-terminal discoidin-like domain through which it self-associates via a head-to-tail mechanism. Human and mouse Muskelin share 98% amino acid seqeuence homology and are encoded by genes located on chromosomes 7q32.3 and 6 A3.3, respectively.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
2-Methyl-2-pentenal (Gemisch der cis- und trans-Isomeren) 97%
Lieferant:
Thermo Scientific
Beschreibung:
EDTA (Ethylendiamintetraessigsäure) 99%, rein
Artikel-Nr:
(BOSSBS-9520R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9520R-CY5
Lokale Artikelnummer::
BOSSBS-9520R-CY5
Beschreibung:
Dyrk (for dual specificity tyrosine phosphorylation regulated kinase) is the homolog of the Drosophila mnb (minibrain) gene, which is required for neurogenesis. Dyrk is a dual-specificity tyrosine kinase and serine/threonine kinase, which is itself regulated by tyrosine phosphorylation. Several mammalian Dyrk related proteins have been identified and are thought to compose a family of dual specificity protein kinases. Dyrk family members, including Dyrk1A (originally Dyrk), Dyrk1B, Dyrk1C, Dyrk2, Dyrk3, Dyrk4A and Dyrk4B, are thought to be involved in diverse cellular functions. Two isoforms of human fetal brain Dyrk2 exist: a deduced 528-amino acid protein and a protein containing 73 additional amino acids at the amino terminus. Dyrk3 is strongly expressed in testis, only after the onset of spermatogenesis, and very weakly expressed in spleen and adrenal gland. The genes which encode Dyrk2 and Dyrk3 map to human chromosomes 12 and 1q32, respectively.
VE:
1 * 100 µl
Lieferant:
BLD PHARMATECH GMBH
Beschreibung:
Moc-Val-OH 98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
EDTA (Ethylendiamintetraessigsäure) ≥99%
Artikel-Nr:
(BOSSBS-5015R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5015R-CY5.5
Lokale Artikelnummer::
BOSSBS-5015R-CY5.5
Beschreibung:
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10150R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10150R-CY7
Lokale Artikelnummer::
BOSSBS-10150R-CY7
Beschreibung:
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10150R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10150R-CY5
Lokale Artikelnummer::
BOSSBS-10150R-CY5
Beschreibung:
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq].
VE:
1 * 100 µl
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