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(2S)-2-(4-Bromophenyl)-2-hydroxyacetic+acid
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(2S)-2-(4-Bromophenyl)-2-hydroxyacetic+acid
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:
(MOLE19502189-500G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
19502189-500G
Lokale Artikelnummer::
MOLE19502189-500G
Beschreibung:
Bromacetaldehyddiethylacetal
VE:
1 * 500 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
Honeywell Chemicals
Beschreibung:
Glyoxalbis(2-hydroxyanil) Indikator für die Metalltitration, Fluka™
Lieferant:
Thermo Scientific
Beschreibung:
Ethylbromdifluoracetat
Artikel-Nr:
(EHERC17324700)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C17324700
Lokale Artikelnummer::
EHERC17324700
Beschreibung:
Tetrabrombisphenol A
VE:
1 * 0,25 g
Lieferant:
Sigma-Aldrich
Beschreibung:
PIPES, Sigma-Aldrich®
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:
(EHERC15981600)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C15981600
Lokale Artikelnummer::
EHERC15981600
Beschreibung:
3-Pentanon
VE:
1 * 1 mL
Artikel-Nr:
(SIALM28006-25G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
M28006-25G
Lokale Artikelnummer::
SIALM28006-25G
Beschreibung:
(Methylamino)acetaldehyddimethylacetal, Sigma-Aldrich®
VE:
1 * 25 g
Lieferant:
Sigma-Aldrich
Beschreibung:
Ethyldifluoracetat, Sigma-Aldrich®
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
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
Artikel-Nr:
(SIAL235334-25G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
235334-25G
Lokale Artikelnummer::
SIAL235334-25G
Beschreibung:
3,6-Dithia-1,8-octandiol, Sigma-Aldrich®
VE:
1 * 25 g
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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