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(5-Chlorobenzo[d][1,3]dioxol-4-yl)boronic+acid
Artikel-Nr:
(BOSSBS-12332R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12332R-A647
Lokale Artikelnummer::
BOSSBS-12332R-A647
Beschreibung:
Dyrk is the homolog of the Drosophila mnb (minibrain) gene, which is required for neurogenesis (1–3). Dyrk is a dual-specificity tyrosine kinase and serine/threonine kinase, which is itself regulated by tyrosine phosphorylation (1). Several mammalian Dyrk related proteins have been identified and are thought to compose a family of dual specificity protein kinases (4). Dyrk family members, including Dyrk1A (originally Dyrk), Dyrk1B, Dryk1C, Dyrk2, Dyrk3, Dyrk4A and Dyrk4B, are thought to be involved in diverse cellular functions (4). Dyrk1A is a candidate gene that may be involved in Downs syndrome, and it has been found to be somewhat overexpressed in Downs syndrome (1,5). 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 (4). Dyrk3 is strongly expressed in testis, only after the onset of spermatogenesis, and very weakly expressed in spleen and adrenal gland (1). The genes which encode Dyrk2 and Dyrk3 map to human chromosomes 12 and 1q32, respectively (4).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12295R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12295R-CY7
Lokale Artikelnummer::
BOSSBS-12295R-CY7
Beschreibung:
Pbx 1, 2, 3 and 4 are members of the TALE (three amino acid loop extension) family of homeodomain-containing proteins. Human pre-B cell acute leukemias are frequently associated with a t(1;19)(q23;p13.3) chromosomal rearrangement, which creates a chimeric gene encoding a fusion between the E2A and Pbx 1 gene products. Pbx 2 and Pbx 3 share 92% and 94% respective identities with Pbx 1 over a 266 amino acid region flanking their homeobox domains, while all three proteins are quite divergent at their amino- and carboxy-termini. Two forms of Pbx 1 and Pbx 3 each differ primarily in their carboxy-termini and result from alternative mRNA splicing. Unlike other homeotic selector genes which are expressed transiently during development and differentiation, Pbx gene transcripts are ubiquitously expressed in both fetal and adult tissues and cell lines. Additionally, Pbx 2 and Pbx 3 transcripts are detected in lymphoid cells, which do not express Pbx 1. Pbx 4 expression is confined to the testis, especially to spermatocytes in the pachytene stage of the first meiotic prophase.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12296R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12296R
Lokale Artikelnummer::
BOSSBS-12296R
Beschreibung:
Pbx 1, 2, 3 and 4 are members of the TALE (three amino acid loop extension) family of homeodomain-containing proteins. Human pre-B cell acute leukemias are frequently associated with a t(1;19)(q23;p13.3) chromosomal rearrangement, which creates a chimeric gene encoding a fusion between the E2A and Pbx 1 gene products. Pbx 2 and Pbx 3 share 92% and 94% respective identities with Pbx 1 over a 266 amino acid region flanking their homeobox domains, while all three proteins are quite divergent at their amino- and carboxy-termini. Two forms of Pbx 1 and Pbx 3 each differ primarily in their carboxy-termini and result from alternative mRNA splicing. Unlike other homeotic selector genes which are expressed transiently during development and differentiation, Pbx gene transcripts are ubiquitously expressed in both fetal and adult tissues and cell lines. Additionally, Pbx 2 and Pbx 3 transcripts are detected in lymphoid cells, which do not express Pbx 1. Pbx 4 expression is confined to the testis, especially to spermatocytes in the pachytene stage of the first meiotic prophase.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12298R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12298R-A680
Lokale Artikelnummer::
BOSSBS-12298R-A680
Beschreibung:
Pbx 1, 2, 3 and 4 are members of the TALE (three amino acid loop extension) family of homeodomain-containing proteins. Human pre-B cell acute leukaemias are frequently associated with a t(1;19)(q23;p13.3) chromosomal rearrangement, which creates a chimeric gene encoding a fusion between the E2A and Pbx 1 gene products. Pbx 2 and Pbx 3 share 92% and 94% respective identities with Pbx 1 over a 266 amino acid region flanking their homeobox domains, while all three proteins are quite divergent at their amino- and carboxy-termini. Two forms of Pbx 1 and Pbx 3 each differ primarily in their carboxy-termini and result from alternative mRNA splicing. Unlike other homeotic selector genes which are expressed transiently during development and differentiation, Pbx gene transcripts are ubiquitously expressed in both fetal and adult tissues and cell lines. Additionally, Pbx 2 and Pbx 3 transcripts are detected in lymphoid cells, which do not express Pbx 1. Pbx 4 expression is confined to the testis, especially to spermatocytes in the pachytene stage of the first meiotic prophase.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13205R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13205R-A350
Lokale Artikelnummer::
BOSSBS-13205R-A350
Beschreibung:
The forkhead domain-containing gene family (Fox) comprises over 20 members in mammals and is defined by a conserved 110 amino-acid motif containing a winged helix structure DNA-binding domain. The members of this gene family have been implicated as key regulators of embryogenesis, cell cycling, cell lineage restriction and cancer. As such, FOXN2 contains a domain with homology to the forkhead DNA binding domain. FOXN2, or Human T-cell leukemia virus enhancer factor, is a 341 amino acid protein mapping to human gene FOXN2, which has been localized to human chromosome 2p16-p22. This protein, encoded by a 1239-bp cDNA isolated from the Jurkat cDNA library, is capable of binding to a region of the human T-cell leukemia virus long terminal repeat (HTLV-I LTR) located between amino acids 155 and 117. This purine-rich region is important in the regulation of gene expression by the Ets family of transcription factors. FOXN2 is a unique cellular gene that may function in the transcriptional regulation of HTLV-I LTR.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13205R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13205R-HRP
Lokale Artikelnummer::
BOSSBS-13205R-HRP
Beschreibung:
The forkhead domain-containing gene family (Fox) comprises over 20 members in mammals and is defined by a conserved 110 amino-acid motif containing a winged helix structure DNA-binding domain. The members of this gene family have been implicated as key regulators of embryogenesis, cell cycling, cell lineage restriction and cancer. As such, FOXN2 contains a domain with homology to the forkhead DNA binding domain. FOXN2, or Human T-cell leukemia virus enhancer factor, is a 341 amino acid protein mapping to human gene FOXN2, which has been localized to human chromosome 2p16-p22. This protein, encoded by a 1239-bp cDNA isolated from the Jurkat cDNA library, is capable of binding to a region of the human T-cell leukemia virus long terminal repeat (HTLV-I LTR) located between amino acids 155 and 117. This purine-rich region is important in the regulation of gene expression by the Ets family of transcription factors. FOXN2 is a unique cellular gene that may function in the transcriptional regulation of HTLV-I LTR.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13451R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13451R-HRP
Lokale Artikelnummer::
BOSSBS-13451R-HRP
Beschreibung:
NP60 is a 553 amino acid nuclear protein that regulates the phosphorylation and activation of p38 alpha in response to stress. There are five isoforms of NP60 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13451R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13451R-A488
Lokale Artikelnummer::
BOSSBS-13451R-A488
Beschreibung:
NP60 is a 553 amino acid nuclear protein that regulates the phosphorylation and activation of p38 alpha in response to stress. There are five isoforms of NP60 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0056R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0056R-A488
Lokale Artikelnummer::
BOSSBS-0056R-A488
Beschreibung:
Insulin decreases blood glucose concentration. It increases cell permeability to monosaccharides, amino acids and fatty acids. It accelerates glycolysis, the pentose phosphate cycle, and glycogen synthesis in liver.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8259R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8259R-CY5
Lokale Artikelnummer::
BOSSBS-8259R-CY5
Beschreibung:
Catalyzes the NAD-dependent oxidative cleavage of spermidine and the subsequent transfer of the butylamine moiety of spermidine to the epsilon-amino group of a specific lysine residue of the eIF-5A precursor protein to form the intermediate deoxyhypusine residue.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8259R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8259R
Lokale Artikelnummer::
BOSSBS-8259R
Beschreibung:
Catalyzes the NAD-dependent oxidative cleavage of spermidine and the subsequent transfer of the butylamine moiety of spermidine to the epsilon-amino group of a specific lysine residue of the eIF-5A precursor protein to form the intermediate deoxyhypusine residue.
VE:
1 * 100 µl
Artikel-Nr:
(USBI167584)
Lieferant:
US Biological
Hersteller-Artikelnummer::
167584
Lokale Artikelnummer::
USBI167584
Beschreibung:
Anti-SLC1A1 Mouse Monoclonal Antibody [clone: S180-41]
VE:
1 * 100 µG
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Fluor-L-phenylalanin 98%
Artikel-Nr:
(BOSSBS-9936R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9936R-A680
Lokale Artikelnummer::
BOSSBS-9936R-A680
Beschreibung:
C11orf21 is a 132 amino acid cytoplasmic protein that is expressed exclusively in heart and is encoded by a gene located on human chromosome 11. Diseases associated with C11orf21 include Beckwith-Wiedemann Syndrome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9936R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9936R-A750
Lokale Artikelnummer::
BOSSBS-9936R-A750
Beschreibung:
C11orf21 is a 132 amino acid cytoplasmic protein that is expressed exclusively in heart and is encoded by a gene located on human chromosome 11. Diseases associated with C11orf21 include Beckwith-Wiedemann Syndrome.
VE:
1 * 100 µl
Artikel-Nr:
(A1348.0100)
Lieferant:
PanReac AppliChem
Hersteller-Artikelnummer::
A1348.0100
Lokale Artikelnummer::
APLIA1348.0100
Beschreibung:
Adenosin-5'-triphosphat Dinatriumsalz (ATP Dinatriumsalz)
VE:
1 * 100 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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