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Methyl+trans-3-hydroxycyclobutanecarboxylate
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Methyl+trans-3-hydroxycyclobutanecarboxylate
Artikel-Nr:
(BOSSBS-11687R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11687R-FITC
Lokale Artikelnummer::
BOSSBS-11687R-FITC
Beschreibung:
PCSK1N is a 260 amino acid protein that is both secreted and localized to the trans-Golgi network. Expressed in pancreas and brain, PCSK1N is thought to play a role in the control of the neuroendocrine secretory pathway and may also be involved in PCSK1 inhibition. The gene encoding PCSK1N maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1,000 genes. In conjunction with chromosome Y, chromosome X is responsible for sex determination, as an X and a Y chromosome lead to normal male development, while two copies of an X chromosome lead to normal female development. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13487R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13487R-HRP
Lokale Artikelnummer::
BOSSBS-13487R-HRP
Beschreibung:
Golgin 245 is also known as p230, GCP2, GOLG or golgi autoantigen and is a 2,230 amino acid protein that is expressed as three isoforms. Golgin 245 is localized to the cytoplasm in cells and is a member of the golgin family, all of which are peripheral membrane proteins associated with the Golgi complex. Golgin 245 has a carboxyl-terminal GRIP domain, which attaches to the trans-Golgi network (TGN) and TGN-derived vesicles. It is thought that the interaction that takes place between golgin 245 and MACF1, which cross-links microtubules to the Actin cytoskeleton, allows proteins to be transported from the TGN to the cell periphery. against golgin 245 are associated with two chronic disorders known as Sjé°ƒren's syndrome and Hepatitis B.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10029R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10029R-HRP
Lokale Artikelnummer::
BOSSBS-10029R-HRP
Beschreibung:
This gene encodes a member of the nectin family. The encoded protein contains two immunoglobulin-like (Ig-like) C2-type domains and one Ig-like V-type domain. It is involved in cell adhesion through trans-homophilic and -heterophilic interactions. It is a single-pass type I membrane protein. The soluble form is produced by proteolytic cleavage at the cell surface by the metalloproteinase ADAM17/TACE. The secreted form is found in both breast tumor cell lines and breast tumor patients. Mutations in this gene are the cause of ectodermal dysplasia-syndactyly syndrome type 1, an autosomal recessive disorder. Alternatively spliced transcript variants have been found but the full-length nature of the variant has not been determined.
VE:
1 * 100 µl
Artikel-Nr:
(SIALD221902-100G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
D221902-100G
Lokale Artikelnummer::
SIALD221902-100G
Beschreibung:
(2-Dodecen-1-yl)bernsteinsäureanhydrid (Gemisch der cis- und trans-Isomeren), Sigma-Aldrich®
VE:
1 * 100 g
Artikel-Nr:
(SIALM13807-100G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
M13807-100G
Lokale Artikelnummer::
SIALM13807-100G
Beschreibung:
4-Methoxyzimtsäure überwiegend trans 99%, Sigma-Aldrich®
VE:
1 * 100 g
Lieferant:
Sigma-Aldrich
Beschreibung:
1,4-Bis(hydroxymethyl)cyclohexan (Gemisch der cis- und trans-Isomeren), Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-11785R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11785R-A750
Lokale Artikelnummer::
BOSSBS-11785R-A750
Beschreibung:
Maspardin is a 308 amino acid cytoplasmic protein that is widely expressed. Belonging to the AB hydrolase superfamily, Maspardin colocalizes with CD4 on endosomal/trans-Golgi network. It is thought that Maspardin may act as a negative regulatory factor in CD4-dependent T-cell activation. Defects in the gene encoding Maspardin are the result of hereditary spastic paraplegia autosomal recessive type 21 (also designated Mast syndrome), an autosomal recessive neurodegenerative disorder characterised by a slow, gradual, progressive weakness and spasticity of the lower limbs. The gene encoding Maspardin is encoded by human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1970R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1970R-FITC
Lokale Artikelnummer::
BOSSBS-1970R-FITC
Beschreibung:
Lysosome associated membrane protein (LAMP1), also known as lgp120 or lgpA, is a type 1 integral membrane protein that is transported from trans Golgi networks to endosomes and then lysosomes. Upon cell activation, LAMP1 transfer to the plasma membrane is dependent on a carboxyl terminal tyrosine based motif (YXXI). Perturbation in the spacing between the tyrosine based motif relative to the membrane abolishes lysosome localization of LAMP1. This mutant protein then cycles between the plasma membrane and the endosome. Cell surface LAMP1 and LAMP2 have been shown to promote adhesion of human peripheral blood mononuclear cells (PBMC) to vascular endothelium, therefore they are possibly involved in the adhesion of PBMCs to the site of inflammation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1970R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1970R-CY7
Lokale Artikelnummer::
BOSSBS-1970R-CY7
Beschreibung:
Lysosome associated membrane protein (LAMP1), also known as lgp120 or lgpA, is a type 1 integral membrane protein that is transported from trans Golgi networks to endosomes and then lysosomes. Upon cell activation, LAMP1 transfer to the plasma membrane is dependent on a carboxyl terminal tyrosine based motif (YXXI). Perturbation in the spacing between the tyrosine based motif relative to the membrane abolishes lysosome localization of LAMP1. This mutant protein then cycles between the plasma membrane and the endosome. Cell surface LAMP1 and LAMP2 have been shown to promote adhesion of human peripheral blood mononuclear cells (PBMC) to vascular endothelium, therefore they are possibly involved in the adhesion of PBMCs to the site of inflammation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11270R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11270R-CY7
Lokale Artikelnummer::
BOSSBS-11270R-CY7
Beschreibung:
HSP56 is a cis-trans prolyl isomerase belonging to the immunophilin protein family. The human HSP 56 gene (FKBP4) has multiple polyadenylation sites and the HSP 56 protein can undergo phosphorylation. HSP 56 influences immunoregulatory gene expression in lymphocytes, protein folding and trafficking. It can serve as a co-chaperone for steroid hormone nuclear receptors to govern appropriate hormone action in target tissues. The protein can associate with phytanoyl-CoA alpha-hydroxylase (PHYH) and with HSP90 through a series of tetratricopeptide repeat (TPR) domains. HSP 56 is a TRPC ion channel accessory protein that modulates channel activation following receptor stimulation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11270R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11270R-A750
Lokale Artikelnummer::
BOSSBS-11270R-A750
Beschreibung:
HSP56 is a cis-trans prolyl isomerase belonging to the immunophilin protein family. The human HSP 56 gene (FKBP4) has multiple polyadenylation sites and the HSP 56 protein can undergo phosphorylation. HSP 56 influences immunoregulatory gene expression in lymphocytes, protein folding and trafficking. It can serve as a co-chaperone for steroid hormone nuclear receptors to govern appropriate hormone action in target tissues. The protein can associate with phytanoyl-CoA alpha-hydroxylase (PHYH) and with HSP90 through a series of tetratricopeptide repeat (TPR) domains. HSP 56 is a TRPC ion channel accessory protein that modulates channel activation following receptor stimulation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2969R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2969R
Lokale Artikelnummer::
BOSSBS-2969R
Beschreibung:
E7 protein has both transforming and trans-activating activities. Disrupts the function of host retinoblastoma protein RB1/pRb, which is a key regulator of the cell cycle. Induces the disassembly of the E2F1 transcription factors from RB1, with subsequent transcriptional activation of E2F1-regulated S-phase genes. Inactivation of the ability of RB1 to arrest the cell cycle is critical for cellular transformation, uncontrolled cellular growth and proliferation induced by viral infection. Stimulation of progression from G1 to S phase allows the virus to efficiently use the cellular DNA replicating machinery to achieve viral genome replication. Interferes with histone deacetylation mediated by HDAC1 and HDAC2, leading to activation of transcription (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(REST30280)
Lieferant:
Restek
Hersteller-Artikelnummer::
30280
Lokale Artikelnummer::
REST30280
Beschreibung:
Organic Standard, trans-1,2-Dichloroethene, 1 ml/ampoule
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-11785R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11785R-HRP
Lokale Artikelnummer::
BOSSBS-11785R-HRP
Beschreibung:
Maspardin is a 308 amino acid cytoplasmic protein that is widely expressed. Belonging to the AB hydrolase superfamily, Maspardin colocalizes with CD4 on endosomal/trans-Golgi network. It is thought that Maspardin may act as a negative regulatory factor in CD4-dependent T-cell activation. Defects in the gene encoding Maspardin are the result of hereditary spastic paraplegia autosomal recessive type 21 (also designated Mast syndrome), an autosomal recessive neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. The gene encoding Maspardin is encoded by human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1970R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1970R-HRP
Lokale Artikelnummer::
BOSSBS-1970R-HRP
Beschreibung:
Lysosome associated membrane protein (LAMP1), also known as lgp120 or lgpA, is a type 1 integral membrane protein that is transported from trans Golgi networks to endosomes and then lysosomes. Upon cell activation, LAMP1 transfer to the plasma membrane is dependent on a carboxyl terminal tyrosine based motif (YXXI). Perturbation in the spacing between the tyrosine based motif relative to the membrane abolishes lysosome localization of LAMP1. This mutant protein then cycles between the plasma membrane and the endosome. Cell surface LAMP1 and LAMP2 have been shown to promote adhesion of human peripheral blood mononuclear cells (PBMC) to vascular endothelium, therefore they are possibly involved in the adhesion of PBMCs to the site of inflammation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13454R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13454R-A555
Lokale Artikelnummer::
BOSSBS-13454R-A555
Beschreibung:
GMEB-1 is a 573 amino acid protein that contains one SAND domain and is a member of the KDWK family of combinatorial transcription modulators. Localized to both the cytoplasm and the nucleus, GMEB-1 forms a heterodimer with GMEB-2 (Glucocorticoid modulatory element-binding protein 2) and, once associated with GMEB-2, plays a key role in parvovirus DNA replication. In addition, GMEB-1 functions alone as a trans-acting factor that, by binding to glucocorticoid modulatory elements (GMEs) in TAT (tyrosine aminotransferase) promoters, increases intracellular sensitivity to glucocorticoid concentrations. GMEB-1 also interacts with initiator procaspases and, via this interaction, can inhibit caspase-induced apoptosis. Due to alternative splicing events, GMEB-1 is expressed as two isoforms.
VE:
1 * 100 µl
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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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