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Dichloromethylenedimethyliminium+chloride
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Dichloromethylenedimethyliminium+chloride
Artikel-Nr:
(SIAL86470-50G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
86470-50G
Lokale Artikelnummer::
SIAL86470-50G
Beschreibung:
p-Terphenyl, Sigma-Aldrich®
VE:
1 * 50 g
Artikel-Nr:
(SIAL700312-5ML)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
700312-5ML
Lokale Artikelnummer::
SIAL700312-5ML
Beschreibung:
It contains <1.0% oleic acid stabilizing ligands.
VE:
1 * 5 mL
Artikel-Nr:
(211-8040)
Lieferant:
SCHAEFER GUENTHER KUNSTSTOF
Hersteller-Artikelnummer::
111540
Lokale Artikelnummer::
SCAE111540
Beschreibung:
Klares Acrylglas.
VE:
1 * 1 ST
Lieferant:
Sigma-Aldrich
Beschreibung:
2-Methyl-2-penten, Sigma-Aldrich®
Lieferant:
DWK Life Sciences
Beschreibung:
EPDM or Vitron.
Artikel-Nr:
(BOSSBS-11956R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11956R-A555
Lokale Artikelnummer::
BOSSBS-11956R-A555
Beschreibung:
The leucine-rich (LRR) repeat is a 20-30 amino acid motif that forms a hydrophobic å/∫ horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. SLITRK3 (SLIT and NTRK-like family, member 3) is a 977 amino acid single-pass type I membrane protein that contains 20 LRR repeats and belongs to the SLITRK family. Expressed at highest levels in cerebral cortex, SLITRK3 is also found in adult and fetal neural tissues and some astrocytic brain tumors. SLITRK3 functions to suppress neurite outgrowth and plays a role in the regulation of neuronal function. SLITRK3 is encoded by a gene that maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6943R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6943R-A555
Lokale Artikelnummer::
BOSSBS-6943R-A555
Beschreibung:
F-box proteins are critical components of the SCF (Skp1-CUL-1-F-box protein) type E3 ubiquitin ligase complex and are involved in substrate recognition and protein recruitment. F-box proteins are members of a large family that regulate the cell cycle, immune response, signaling cascades and developmental programs by targeting proteins, such as cyclins, for degradation by the proteasome after ubiquitination. FBL11, also known as FBXL11 (F-box and leucine-rich repeat protein 11), CXXC8, KDM2A, JHDM1A (JmjC domain-containing histone demethylation protein 1A) or LILINA, is a 1,162 amino acid member of the F-box protein family that contains one F-box domain and localizes to the nucleus. Expressed ubiquitously with highest expression in testis, ovary and brain, FBL11 functions to demethylate the Lys-36 residue of histone H3, thereby modulating the histone code. Additionally, FBL11 is thought to promote the ubiquitination and subsequent degradation of various phosphorylated proteins. Three isoforms of FBL11 exist due to alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(HECH42808033)
Lieferant:
GLASWARENFABRIK KARL HECHT
Hersteller-Artikelnummer::
42808033
Lokale Artikelnummer::
HECH42808033
Beschreibung:
Test tube racks, made of Plexiglas®, with numbered holes.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-9212R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9212R-A750
Lokale Artikelnummer::
BOSSBS-9212R-A750
Beschreibung:
The serine proteinase inhibitors (serpins) compose a superfamily of proteins with a diverse set of functions, including the control of blood coagulation, complement activation, programmed cell death and development. Serpins are secreted glycoproteins that contain a stretch of peptide that mimics a true substrate for a corresponding serine protease. SerpinB11 (serpin peptidase inhibitor, clade B (ovalbumin), member 11), also known as EPIPIN or SERPIN11, is a 392 amino acid cytoplasmic protein that belongs to the Ov-serpin subfamily and serpin family. Like other members of the serpin family, SerpinB11 has been identified as a noninhibitory intracellular protein. The gene encoding SerpinB11 maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localised genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
VE:
1 * 100 µl
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-11771R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11771R-FITC
Lokale Artikelnummer::
BOSSBS-11771R-FITC
Beschreibung:
SCA11 is a 1,244 amino acid protein that belongs to the protein kinase superfamily and the CK1 Ser/Thr protein kinase family. The SCA11 gene, comprising of 16 exons, produces a 5.6-kb transcript in which the longest open reading frame is 3,732 nucleotides. Defects in the SCA11 protein are the cause of the disorder spinocerebellar ataxia type 11 (SCA11). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. The SCA11 disorder is an autosomal dominant cerebellar ataxia (ADCA). It is a relatively benign, late-onset, slowly progressive neurologic disorder. The SCA11 protein has also been implicated in Alzheimer disease and in tangle formation. Existing as three alternatively spliced isoforms, the SCA11 gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 15q15.2.
VE:
1 * 100 µl
Artikel-Nr:
(221-0038)
Lieferant:
SciLabware
Hersteller-Artikelnummer::
FWC104
Lokale Artikelnummer::
AZLOFWC104
Beschreibung:
HDPE, durchscheinend.
VE:
1 * 10 ST
Artikel-Nr:
(BOSSBS-12311R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12311R-A488
Lokale Artikelnummer::
BOSSBS-12311R-A488
Beschreibung:
The leucine-rich (LRR) repeat is a 20-30 amino acid motif that forms a hydrophobic å/∫ horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. The primary function of these motifs is to provide a versatile structural framework to mediate the formation of protein-protein interactions. LRRs are present in a variety of proteins with diverse structure and function, including innate immunity and nervous system development. Several human diseases are associated with mutations in genes encoding LRR-containing proteins. LRRC23 (leucine-rich repeat-containing protein 23), also known as leucine-rich protein B7, is a 343 amino acid protein that contains eight LRR (leucine-rich) repeasts and one LRRCT domain. LRRC23 exists as two alternatively spliced isoforms and is encoded by a gene mapping to chromosome 12.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11771R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11771R-HRP
Lokale Artikelnummer::
BOSSBS-11771R-HRP
Beschreibung:
SCA11 is a 1,244 amino acid protein that belongs to the protein kinase superfamily and the CK1 Ser/Thr protein kinase family. The SCA11 gene, comprising of 16 exons, produces a 5.6-kb transcript in which the longest open reading frame is 3,732 nucleotides. Defects in the SCA11 protein are the cause of the disorder spinocerebellar ataxia type 11 (SCA11). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. The SCA11 disorder is an autosomal dominant cerebellar ataxia (ADCA). It is a relatively benign, late-onset, slowly progressive neurologic disorder. The SCA11 protein has also been implicated in Alzheimer disease and in tangle formation. Existing as three alternatively spliced isoforms, the SCA11 gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 15q15.2.
VE:
1 * 100 µl
Artikel-Nr:
(HACH2067299)
Lieferant:
Hach
Hersteller-Artikelnummer::
2067299
Lokale Artikelnummer::
HACH2067299
Beschreibung:
Thymolblau
VE:
1 * 100 ST
Artikel-Nr:
(630-0081)
Lieferant:
MOTIC
Hersteller-Artikelnummer::
1101001400572
Lokale Artikelnummer::
MOTI1101001400572
Beschreibung:
Diese Hellfeldmikroskope sind für Anwendungen im Bildungswesen konzipiert.
VE:
1 * 1 ST
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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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