H-Tyr(BZL)-OMe·HCl
Artikel-Nr:
(MOLEM70152720)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M70152720
Lokale Artikelnummer::
MOLEM70152720
Beschreibung:
Natriumacetat Trihydrat
VE:
1 * 1 kg
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Lieferant:
MP Biomedicals
Beschreibung:
Potassium acetate is utilized in the isolation of RNA intermediates and products from in vitro splicing reactions performed with a HeLa cell nuclear extract.Potassium acetate is used as a buffer in molecular biology research, notably in the isolation of DNA.
Lieferant:
Honeywell Chemicals
Beschreibung:
Ammoniumacetat ≥99,0% (durch Trockensubstanz) für die HPLC, Fluka™
Artikel-Nr:
(BOSSBS-12330R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12330R-A647
Lokale Artikelnummer::
BOSSBS-12330R-A647
Beschreibung:
The tripartite motif (TRIM) family of proteins are characterized by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. Staf-50 (50 kDa-stimulated trans-acting factor), also known as TRIM22 (tripartite motif-containing 22), RNF94 or GPSTAF50, is a 498 amino acid cytoplasmic protein that belongs to the TRIM family and, characteristic of TRIM family members, contains one RING-type zinc finger, one B box-type zinc finger and one SPRY domain. Induced by IFN-å and IFN-∫, Staf-50 is strongly expressed in ovary, spleen, thymus and peripheral blood leukocytes where it is thought to mediate the antiviral effects of IFN proteins. Additionally, Staf-50 is present in leukemic cells, suggesting a role in cancer formation and metastasis. Staf-50 exists as two alternatively spliced isoforms which are encoded by a gene that maps to human chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15350R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15350R
Lokale Artikelnummer::
BOSSBS-15350R
Beschreibung:
C9orf96, also known as Protein kinase-like protein SgK071, is a 680 amino acid protein that belongs to the Ser/Thr protein kinase family of the protein kinase superfamily. There are three isoforms of C9orf96 that are produced as a result of alternative splicing events. The gene encoding C9orf96 maps to human chromosome 9, which consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(SIALR856-100G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
R856-100G
Lokale Artikelnummer::
SIALR856-100G
Beschreibung:
Resorcinmonoacetat, Sigma-Aldrich®
VE:
1 * 100 g
Artikel-Nr:
(BOSSBS-13536R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13536R-A680
Lokale Artikelnummer::
BOSSBS-13536R-A680
Beschreibung:
G protein-coupled receptor that is activated by a major product of dietary fiber digestion, the short chain fatty acids (SCFAs), and that plays a role in the regulation of whole-body energy homeostasis and in intestinal immunity. In omnivorous mammals, the short chain fatty acids acetate, propionate and butyrate are produced primarily by the gut microbiome that metabolizes dietary fibers. SCFAs serve as a source of energy but also act as signaling molecules. That G protein-coupled receptor is probably coupled to the pertussis toxin-sensitive, G(i/o)-alpha family of G proteins but also to the Gq family (PubMed:12496283, PubMed:12711604, PubMed:23589301). Its activation results in the formation of inositol 1,4,5-trisphosphate, the mobilization of intracellular calcium, the phosphorylation of the MAPK3/ERK1 and MAPK1/ERK2 kinases and the inhibition of intracellular cAMP accumulation. May play a role in glucose homeostasis by regulating the secretion of GLP-1, in response to short-chain fatty acids accumulating in the intestine. May also regulate the production of LEP/Leptin, a hormone acting on the central nervous system to inhibit food intake. Finally, may also regulate whole-body energy homeostasis through adipogenesis regulating both differentiation and lipid storage of adipocytes. In parallel to its role in energy homeostasis, may also mediate the activation of the inflammatory and immune responses by SCFA in the intestine, regulating the rapid production of chemokines and cytokines. May also play a role in the resolution of the inflammatory response and control chemotaxis in neutrophils. In addition to SCFAs, may also be activated by the extracellular lectin FCN1 in a process leading to activation of monocytes and inducing the secretion of interleukin-8/IL-8 in response to the presence of microbes (PubMed:21037097).
VE:
1 * 100 µl
Lieferant:
Sigma-Aldrich
Beschreibung:
Natriumacetat Trihydrat, Sigma-Aldrich®
Artikel-Nr:
(J62557.MB)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
J62557.MB
Lokale Artikelnummer::
ALFAJ62557.MB
Beschreibung:
DL-Thiorphan
VE:
1 * 25 mg
Artikel-Nr:
(MENANC127.25)
Lieferant:
MENAI
Hersteller-Artikelnummer::
NC127.25
Lokale Artikelnummer::
MENANC127.25
Beschreibung:
(4-Fluorphenoxy)essigsäurehydrazid
VE:
1 * 25 g
Artikel-Nr:
(ICNA0219502305)
Lieferant:
MP Biomedicals
Hersteller-Artikelnummer::
0219502305
Lokale Artikelnummer::
ICNA0219502305
Beschreibung:
2,2-Azino-bis-(3-ethyl-benzthiazoline-6-sulfonic acid) (ABTS) has been used as a chromogenic substrate for horseradish peroxidase (HRP), both in general activity assays and in ELISA applications. Activity of HRP using ABTS appears about four-fold higher than using pyrogallol. It is mainly used as a substrate in sensitive peroxidase assays.
2,2′-Azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) is a peroxidase substrate suitable for use in ELISA procedures. This substrate produces a soluble end product that is green in color and can be read spectrophotometrically at 405 nm. The reaction may be stopped with 1% sodium dodecyl sulfate (SDS). Recommended for ELISA (microwell) procedures, not recommended for membrane applications.
VE:
1 * 5 g
Lieferant:
FLUOROCHEM
Beschreibung:
5-Fluor-3-indolylessigsäure
Lieferant:
Sigma-Aldrich
Beschreibung:
Isoamylacetat, Sigma-Aldrich®
Lieferant:
Thermo Scientific
Beschreibung:
Natriumacetat Trihydrat für die HPLC
Artikel-Nr:
(BOSSBS-9747R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9747R-A647
Lokale Artikelnummer::
BOSSBS-9747R-A647
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD20A (ankyrin repeat domain-containing protein 20A) is an 823 amino acid protein that contains five ANK repeats. The gene encoding ANKRD20A maps to chromosome 9, which consists of about 145 million bases and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and familial dysautonomia are associated with chromosome 9. Also, chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15318R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15318R-A647
Lokale Artikelnummer::
BOSSBS-15318R-A647
Beschreibung:
C9orf169 (chromosome 9 open reading frame 169) is a 423 amino acid single-pass membrane protein that belongs to the clpA/clpB family and torsin subfamily. The gene encoding C9orf169 maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Preis auf Anfrage
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