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5-Amino-1H-indole-3-carboxamide+hydrochloride
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5-Amino-1H-indole-3-carboxamide+hydrochloride
Artikel-Nr:
(BOSSBS-9984R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9984R-A680
Lokale Artikelnummer::
BOSSBS-9984R-A680
Beschreibung:
Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukaemia. The C22orf25 gene product has been provisionally designated C22orf25 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0693R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0693R-A350
Lokale Artikelnummer::
BOSSBS-0693R-A350
Beschreibung:
The membrane-bound isoform 1 is a receptor involved in the development of the cardiovascular system, in angiogenesis, in the formation of certain neuronal circuits and in organogenesis outside the nervous system. It mediates the chemorepulsant activity of semaphorins. It binds to semaphorin 3A, The PLGF-2 isoform of PGF, The VEGF-165 isoform of VEGF and VEGF-B. Coexpression with KDR results in increased VEGF-165 binding to KDR as well as increased chemotaxis. It may regulate VEGF-induced angiogenesis. The soluble isoform 2 binds VEGF-165 and appears to inhibit its binding to cells. It may also induce apoptosis by sequestering VEGF-165. May bind as well various members of the semaphorin family. Its expression has an averse effect on blood vessel number and integrity.
VE:
1 * 100 µl
Artikel-Nr:
(VWRS25642.550)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRS25642.550
Beschreibung:
Ethylmethylketon ≥99,5%, AnalaR NORMAPUR® ACS, Reag. Ph. Eur. analytisches Reagens
VE:
1 * 200 L
Artikel-Nr:
(BLDPBD216796-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD216796-1G
Lokale Artikelnummer::
BLDPBD216796-1G
Beschreibung:
(3S,4R)-1-tert-Butyl 3-ethyl 4-hydroxypyrrolidine-1,3-dicarboxylate 98%
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-9548R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9548R-CY5
Lokale Artikelnummer::
BOSSBS-9548R-CY5
Beschreibung:
Mammalian protein farnesyl transferases are heterodimeric proteins containing two nonidentical Alpha and beta subunits that attach farnesyl residues to a cysteine at the fourth position from the COOH terminus of several proteins, including nuclear lamins and p21Ras proteins. The natural substrates contain the Cys-A-A-Xaa recognition sequence, where the A residues are aliphatic and Xaa represents methionine, serine, glutamine or cysteine. The purified farnesyl transferase is an a-b heterodimer. The beta subunit, which is known as FT beta, CAAX farnesyltransferase subunit beta, or Ras proteins prenyltransferase subunit beta, is a 437 amino acid protein that contains five PFTB repeats and binds the peptide substrate. The Alpha subunit is suspected to participate in formation of a stable complex with the substrate farnesyl pyrophosphate.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15047R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15047R-CY7
Lokale Artikelnummer::
BOSSBS-15047R-CY7
Beschreibung:
C1orf187, also known as Draxin, Dorsal repulsive axon guidance protein and Neucrin, is a 349 amino acid secreted protein that is required of the development of the spinal cord and forebrain commissures. C1orf187 acts as a chemorepulsive guidance protein and directs commissural axons during development by repelling neurite outgrowth from the spinal cord. During development, C1orf187 modulates neural crest migration by reducing the polarization of these cells, leading to reduced velocity of migration and increased frequency of changing direction, leading to a net decrease in migrational distance. It acts as an antagonist of the Wnt signaling pathway by inhibiting the stabilization of cytosolic _-catenin via its interaction with LRP6. C1orf187 inhibits outgrowth from the olfactory bulb and likely contributes to the formation of the lateral olfactory tract.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11778R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11778R
Lokale Artikelnummer::
BOSSBS-11778R
Beschreibung:
Dorfin is a multi-pass membrane, RING-IBR type, E3 ubiquitin-protein ligase. It is widely expressed with highest levels found in heart and ubiquitous expression throughout the central nervous system. Dorfin functions by accepting ubiquitin in the form of a thioester from UBCH7 and UBC8 and then transferring it to the targeted substrates. Dorfin is responsible for ubiquitylating synphilin-1, CaSR and mutant variants of SOD-1, a protein at fault for familial ALS (amyotrophic lateral sclerosis). Dorfin physically interacts with VCP (Valosin-containing protein) via its C-terminus. Together these two proteins are associated with the formation of ubiquitylated inclusions (UBIs) that characterize many neurodegenerative disorders, such as Parkinson’s disease and ALS. This association with UBIs suggests that Dorfin plays an important role in the disease process.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11111R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11111R-CY7
Lokale Artikelnummer::
BOSSBS-11111R-CY7
Beschreibung:
Protocadherins are a subfamily of cadherins, a large group of related glycoproteins that mediate calcium-dependent cell-to-cell adhesion via a homophilic mechanism. Involved in a variety of functions, protocadherins help to regulate neural development and synapse formation. PCDH1 is a 1,026 amino acid single-pass type I membrane protein that contains seven cadherin domains and is a member of the protocadherin family. Localized to cell-cell and cell-matrix boundaries and expressed at high levels in brain and neuro-glial cells, PCDH1 is thought to be involved in cell adhesion and cell-cell interactions and may play a role in neuronal development. PCDH1 contains a C-terminal cytoplasmic region, an extracellular region and a transmembrane region, and is expressed as two isoforms due to alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8866R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8866R-CY3
Lokale Artikelnummer::
BOSSBS-8866R-CY3
Beschreibung:
Enzymes known as phosphatidylserine decarboxylases (PSDs) catalyze the formation of phosphatidylethanolamine from phosphatidylserine via phosphatidylserine decarboxylation. Type I PSDs contain LGST motifs and are found in bacteria and eukaryotic mitochondria, whereas type II PSDs contain GGST motifs and are found in eukaryotic endomembrane systems. PISD (phosphatidylserine decarboxylase), also known as phosphatidylserine decarboxylase proenzyme, PSDC, PSD, PSSC, DJ858B16, dJ858B16.2 or DKFZp566G2246, is a 408 amino acid a type I phosphatidylserine decarboxylase that localizes to the inner mitochondrial membrane. PISD contains a conserved LGST motif which is cleaved to produce two isoforms known as PISD α and PISD β. PISD is capable of forming a heterodimer and is highly expressed in liver and testis. The gene encoding PISD maps to human chromosome 22q12.2.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9073R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9073R-CY5
Lokale Artikelnummer::
BOSSBS-9073R-CY5
Beschreibung:
C22orf31, also known as HS747E2A or bK747E2.1, is a 290 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11202R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11202R-CY3
Lokale Artikelnummer::
BOSSBS-11202R-CY3
Beschreibung:
NR2 proteins are a large family of nuclear hormone receptor transcription factors. The proteins belonging to this family are characterized by discrete domains functioning in DNA and ligand binding. NR2E1 (nuclear receptor subfamily 2, group E, member 1), also known as TLX, is an essential component in the formation of synaptic plasticity and dendritic structure in retinal astrocytes. In addition, NR2E1 is a orphan receptor that binds DNA as part of the hormone response element (HRE), a transcription regulator for hormones. DNA-binding orphan receptors have the conserved sequence 5'-AAGGTCA-3', a motif that determines substrate binding specificity. NR2E1 is expressed in brain tissue, with highest levels in astrocytes, and is localized to the nucleus. Mutations in the gene that encodes NR2E1 may lead to retinal dystrophy, a disorder characterized by a reduction in the thickness of the retina.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD767301-100MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD767301-100MG
Lokale Artikelnummer::
BLDPBD767301-100MG
Beschreibung:
5-tert-Butyl 3a-ethyl hexahydro-1H-pyrrolo[3,2-c]pyridine-3a,5(6H)-dicarboxylate 97%
VE:
1 * 100 mg
Artikel-Nr:
(BOSSBS-11712R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11712R
Lokale Artikelnummer::
BOSSBS-11712R
Beschreibung:
The charged multivesicular body proteins, commonly designated CHMPs, belong to the vacuolar sorting protein family and function as chromatin-modifying proteins. CHMP1-6 are all components of ESCRT (endosomal sorting complex required for transport) I, II or III complexes. These complexes are crucial for sorting endosomal articles into multivesicular bodies (MVBs), and are also required for the formation of these bodies. CHMP2B, also known as CHMP2.5 or vacuolar protein-sorting-associated protein 2-2, is a 213 amino acid cytosolic protein. Widely expressed in brain, heart, skeletal muscle, small intestine, pancreas, lung, placenta and leukocytes, CHMP2B associates directly with CHMP2A and vps4 for the disassembly of the ESCRT-III complex. Defects in the gene encoding CHMP2B have been shown to cause chromosome 3-linked frontotemporal dementia (FTD3).
VE:
1 * 100 µl
Lieferant:
Merck
Beschreibung:
EMSURE® grade solvents are suitable for a broad spectrum of classical lab applications, and are frequently used in regulated and highly demanding lab applications. EMSURE® provides worldwide best and most extensive product specifications. We declare our EMSURE® range to be in compliance with the ACS, with the reagent part of the European Pharmacopoeia (Reag. Ph Eur) and also with the ISO standards.
Artikel-Nr:
(BLDPBD00813079-250)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD00813079-250
Lokale Artikelnummer::
BLDPBD00813079-250
Beschreibung:
3-Bromo-pyrrolo[1,2-a]pyrimidine-6-carboxylic acid ethyl ester 96%
VE:
1 * 250 mg
Artikel-Nr:
(APOSOR29906-50MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR29906-50MG
Lokale Artikelnummer::
APOSOR29906-50MG
Beschreibung:
Ethyl {[5-(2,6-dichloropyridin-4-yl)-4-methyl-4H-1,2,4-triazol-3-yl]thio}acetate
VE:
1 * 50 mg
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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