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2-Methoxypyrimidine-5-carbonitrile
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2-Methoxypyrimidine-5-carbonitrile
Artikel-Nr:
(PRSI79-138)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
79-138
Lokale Artikelnummer::
PRSI79-138
Beschreibung:
Progesterone receptors (PRs) are nuclear hormone receptors of the NR3C class, which also includes mineralocorticoid, glucocorticoid and androgen receptors. They exist as homodimers coupled to Hsp90 or HMGB proteins, which are shed upon activation. The major signaling pathway used by progesterone receptors is via direct DNA binding and transcriptional regulation of target genes. They can also signal by binding to other proteins, mainly with transcription factors such as NF-κB, AP-1 or STAT. Progesterone receptors are found in the female reproductive tract, mammary glands, brain and pituitary gland and receptor expression is induced by estrogen. Well established functions of progesterone receptors include ovulation, implantation, mammary gland development and maintenance of pregnancy. In addition, progesterone, signaling through the progesterone receptor, increases the ventilatory response of the respiratory centers to carbon dioxide and decreases arterial and alveolar PCO2 in the luteal phase of the menstrual cycle and during pregnancy. The human gene encoding the progesterone receptor has been localized to 11q22.
VE:
1 * 100 µG
Lieferant:
Honeywell Chemicals
Beschreibung:
Glyoxalbis(2-hydroxyanil) Indikator für die Metalltitration, Fluka™
Artikel-Nr:
(MOLE14988162-500G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
14988162-500G
Lokale Artikelnummer::
MOLE14988162-500G
Beschreibung:
BIS-TRIS-Propan
VE:
1 * 500 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(PRSI92-266)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
92-266
Lokale Artikelnummer::
PRSI92-266
Beschreibung:
Interleukin-22(IL-22) is a member of a group of the IL-10 family, a class of potent mediators of cellular inflammatory responses. IL-22 is produced by activated DC and T cells. IL-22 and IL-10 receptor chains play a role in cellular targeting and signal transduction. It can initiate and regulate innate immune responses against bacterial pathogens especially in epithelial cells such as respiratory and gut epithelial cells. IL-22 along with IL-17 likely plays a role in the coordinated response of both adaptive and innate immune systems. IL-22 also promotes hepatocyte survival in the liver and epithelial cells in the lung and gut similar to IL-10. Biological activity of IL-22 is initiated by binding to a cell-surface complex consisting of IL-22R1 and IL-10R2 receptor chains. IL-22 biological activity is further regulated by interactions with a soluble binding protein, IL-22BP. IL-22BP and an extracellular region of IL-22R1 share sequence similarity. In some cases, the pro-inflammatory versus tissue-protective functions of IL-22 are regulated by cytokine IL-17A.
VE:
1 * 50 µG
Artikel-Nr:
(HEWL5190-1484)
Lieferant:
Agilent
Hersteller-Artikelnummer::
5190-1484
Lokale Artikelnummer::
HEWL5190-1484
Beschreibung:
Spritzen, Chromatographie, HPLC/GC, Fixed needle, Volumen: 10 µl, Spitzentyp: LC, Gauge: 22, Länge: 51 mm, VE: 1
VE:
1 * 1 ST
Lieferant:
Sigma-Aldrich
Beschreibung:
PIPES, Sigma-Aldrich®
Artikel-Nr:
(PROOMM0025.07)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
MM0025.07
Lokale Artikelnummer::
PROOMM0025.07
Beschreibung:
Ethyl-diphenylacetat
VE:
1 * 100 mg
Artikel-Nr:
(SIALM28006-25G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
M28006-25G
Lokale Artikelnummer::
SIALM28006-25G
Beschreibung:
(Methylamino)acetaldehyddimethylacetal, Sigma-Aldrich®
VE:
1 * 25 g
Artikel-Nr:
(BOSSBS-15318R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15318R-A680
Lokale Artikelnummer::
BOSSBS-15318R-A680
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
Artikel-Nr:
(BOSSBS-9747R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9747R-A488
Lokale Artikelnummer::
BOSSBS-9747R-A488
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-9747R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9747R-A555
Lokale Artikelnummer::
BOSSBS-9747R-A555
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-9747R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9747R-A750
Lokale Artikelnummer::
BOSSBS-9747R-A750
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 characterised 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 leukaemias.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
Ethylbromdifluoracetat
Artikel-Nr:
(EHERC17324700)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C17324700
Lokale Artikelnummer::
EHERC17324700
Beschreibung:
Tetrabrombisphenol A
VE:
1 * 0,25 g
Artikel-Nr:
(BOSSBS-15350R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15350R-CY7
Lokale Artikelnummer::
BOSSBS-15350R-CY7
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 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
Lieferant:
Sigma-Aldrich
Beschreibung:
Ethyldifluoracetat, Sigma-Aldrich®
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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