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cis-6-Amino-cyclohex-3-enecarboxylic+acid
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cis-6-Amino-cyclohex-3-enecarboxylic+acid
Artikel-Nr:
(GHS132-1L)
Lieferant:
SIGMA ALDRICH MICROSCOPY
Hersteller-Artikelnummer::
GHS132-1L
Lokale Artikelnummer::
SIAMGHS132-1L
Beschreibung:
Gill no.1 formulation is used as a progressive cytology stain.
VE:
1 * 1 L
Artikel-Nr:
(GHS116-500ML)
Lieferant:
SIGMA ALDRICH MICROSCOPY
Hersteller-Artikelnummer::
GHS116-500ML
Lokale Artikelnummer::
SIAMGHS116-500ML
Beschreibung:
Gill No. 1 formulation is used as a progressive cytology stain. Used with hematoxylin and eosin staining.
VE:
1 * 500 mL
Artikel-Nr:
(EHERC15350000)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C15350000
Lokale Artikelnummer::
EHERC15350000
Beschreibung:
cis-9-Tricosen (Muscalur)
VE:
1 * 0,1 g
Artikel-Nr:
(BOSSBS-11703R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11703R-HRP
Lokale Artikelnummer::
BOSSBS-11703R-HRP
Beschreibung:
FMR2 is a 1311 amino acid nuclear protein belonging to the AF4 family. Expressed in the brain, placenta and lung, FMR2 exists as two isoforms produced by alternative splicing. Defects in the gene that encodes FMR2 have been found to be a cause of FRAXE, an X-linked form of mental retardation. Individuals expressing the FRAXE site also have more than two-hundred copies of a GCC repeat adjacent to CpG island, compared to six to thirty-five copies of the GCC repeat in a normal individual. It is believed that loss of FMR2 expression causes this GCC expansion of the FRAXE site.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9414R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9414R-FITC
Lokale Artikelnummer::
BOSSBS-9414R-FITC
Beschreibung:
NET-4, also known as TSPAN5 or TM4SF9, is a 268 amino acid multi-pass membrane protein that belongs to the tetraspanin family and is thought to play a role in signal transduction events related to cell development, activation, growth and motility. The gene encoding NET-4 maps to human chromosome 4, which encodes nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9712R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9712R-A488
Lokale Artikelnummer::
BOSSBS-9712R-A488
Beschreibung:
Na+/H+ exchangers (NHEs) catalyze the transport of Na+ in exchange for H+ across membranes in organisms and are required for numerous physiological processes. NHEDC2 (Na+/H+ exchanger-like domain-containing protein 2), also known as NHA2, is a 537 amino acid mitochondrial protein. NHEDC2 is involved in organelle volume homeostasis by catalyzing the exchange of protons for Na+ and Li+ across the inner mitochondrial membrane. Found in red blood cells, NHEDC2 is required for bone resorption activity and osteoclast differentiation. As a multi-pass membrane protein, NHEDC2 is expressed as two isoforms produced by alternative splicing events.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
2-[Bis(2-hydroxyethyl)amino]ethansulfonsäure 99+% für die Biochemie
Artikel-Nr:
(BOSSBS-12357R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12357R-HRP
Lokale Artikelnummer::
BOSSBS-12357R-HRP
Beschreibung:
CFDP1 is a 299 amino acid protein that is involved in embryogenesis and normal cell function. When treated with CFDP1 peptide, mouse molar teeth increase in size, whereas treating cells with against CFDP1 shows an increase in the number of apoptotic cells and gradual tooth disintegration. CFDP1 is highly expressed in developing mouse teeth and is expressed at lower levels in liver, lung and heart. The gene encoding CFDP1 maps to human chromsome 16, in a region that has been associated with inherited craniofacial diseases, such as fanconi anemia type A. There are two isoforms of CFDP1 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11967R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11967R-A555
Lokale Artikelnummer::
BOSSBS-11967R-A555
Beschreibung:
SRPX2 is a 465 amino acid secreted protein expressed in neurons of the brain, including the rolandic area. It has been suggested that SRPX2 enhances cell motility, migration and adhesion through FAK signaling in gastric and other cancer cells. Localized to the cytoplasm, SRPX2 is a ligand for uPAR (urokinase plasminogen activator), a receptor that is a crucial component of the extracellular plasminogen proteolysis system. SRPX2 may be responsible for rolandic seizures (RSs) associated with oral and speech dyspraxia and mental retardation (MR). The involvement of SRPX2 in these disorders suggests an important role for SRPX2 in the perisylvian region critical for language and cognitive development.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1012R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1012R-A488
Lokale Artikelnummer::
BOSSBS-1012R-A488
Beschreibung:
BMP2 belongs to the transforming growth factor-beta (TGFB) superfamily of secreted growth factors. It is a disulfide-linked homodimer and induces bone and cartilage formation. In addition to its osteogenic activity, BMP2 plays an important role in cardiac morphogenesis and is expressed in a variety of tissues including lung, spleen, brain, liver, prostate ovary and small intestine. The functional form of BMP2 is a 26 kDa protein composed of two identical 114 amino acid polypeptide chains linked by a single disulfide bond. BMPs control fundamental events in early embryonic development, organogenesis and adult tissue homeostasis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12357R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12357R-A488
Lokale Artikelnummer::
BOSSBS-12357R-A488
Beschreibung:
CFDP1 is a 299 amino acid protein that is involved in embryogenesis and normal cell function. When treated with CFDP1 peptide, mouse molar teeth increase in size, whereas treating cells with against CFDP1 shows an increase in the number of apoptotic cells and gradual tooth disintegration. CFDP1 is highly expressed in developing mouse teeth and is expressed at lower levels in liver, lung and heart. The gene encoding CFDP1 maps to human chromsome 16, in a region that has been associated with inherited craniofacial diseases, such as fanconi anemia type A. There are two isoforms of CFDP1 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13043R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13043R-A350
Lokale Artikelnummer::
BOSSBS-13043R-A350
Beschreibung:
The gene encoding DYX1C1 maps in the 15q21 region, which is disrupted by a translocation t(2;15)(q11;q21) and segregates with dyslexia. Two sequence changes in DYX1C1, including one involving the translation initiation sequence and an Elk-1 transcription factor binding site (-3G -->A) and a codon (1249G -->T), introduce a premature stop codon and truncate the protein by 4 amino acids. DYX1C1 encodes a nuclear tetratricopeptide repeat domain protein that is dynamically regulated in brain. In human brain, DYX1C1 protein localizes to a fraction of cortical neurons and white matter glial cells. It is also expressed in lung, kidney and testis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11967R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11967R-HRP
Lokale Artikelnummer::
BOSSBS-11967R-HRP
Beschreibung:
SRPX2 is a 465 amino acid secreted protein expressed in neurons of the brain, including the rolandic area. It has been suggested that SRPX2 enhances cell motility, migration and adhesion through FAK signaling in gastric and other cancer cells. Localized to the cytoplasm, SRPX2 is a ligand for uPAR (urokinase plasminogen activator), a receptor that is a crucial component of the extracellular plasminogen proteolysis system. SRPX2 may be responsible for rolandic seizures (RSs) associated with oral and speech dyspraxia and mental retardation (MR). The involvement of SRPX2 in these disorders suggests an important role for SRPX2 in the perisylvian region critical for language and cognitive development.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13461R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13461R-A488
Lokale Artikelnummer::
BOSSBS-13461R-A488
Beschreibung:
GMPPB is a 360 amino acid protein that belongs to the transferase hexapeptide repeat family and is involved in protein modification pathways. Functioning as a GDP-mannose pyrophosphorylase, GMPPB enzymatically catalyzes the conversion of mannose-1-phosphate and GTP to GDP-mannose and a free phosphate, a reaction that is involved in the production of N-linked oligosaccharides. Defects in the gene encoding GMPPB that cause errors in the glycosylation pathway may lead to congenital disorders of glycosylation (CDG). CDGs are multisystemic diseases that often involve both the central and peripheral nervous systems and are often characterized by endocrine and coagulation disorders. GMPPB is expressed as two isoforms due to alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12907R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12907R-A647
Lokale Artikelnummer::
BOSSBS-12907R-A647
Beschreibung:
BTBD14A is a 587 amino acid protein that contains one BTB/POZ domain. The BTB/POZ domain mediates homomeric and heteromeric POZ-POZ interactions and is common to transcriptional regulators involved in chromatin modeling. In several BTB/POZ containing proteins, including BCL-6 and the promyelocytic leukemia zinc-finger (PLZF) oncoprotein, this domain interacts with the SMRT/N-CoR-mSin3A HDAC complex and is directly involved in repressing and silencing gene transcription. When this domain is deleted, as with the oncogenic PLZF-RAR chimera of promyelocytic leukemias, this transcriptional repression is attenuated. This suggests that BTBD14A may play a role in transcription regulation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13570R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13570R
Lokale Artikelnummer::
BOSSBS-13570R
Beschreibung:
The BTB is an N-terminal homodimerization domain that contains multiple copies of kelch repeats and/or C2H2-type zinc fingers. Proteins that contain BTB domains are thought to be involved in transcriptional regulation via control of chromatin structure and function. ZBTB3 (zinc finger and BTB domain containing 3) is a 574 amino acid protein that contains one BTB (POZ) domain and two C2H2-type zinc fingers. Localized to the nucleus, ZBTB3 is thought to play a role in transcriptional regulation events. The gene encoding ZBTB3 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome.
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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