Suche >
Drucken
Lieferant:
Alfa Aesar
Beschreibung:
Cer ≥99,8% (REO, Basis der Oxide der Metalle der seltenen Erden), Barren
Artikel-Nr:
(BOSSBS-6258R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6258R-CY5
Lokale Artikelnummer::
BOSSBS-6258R-CY5
Beschreibung:
A reciprocal translocation between chromosomes 22 and 9 produces the Philadelphia chromosome, which is often found in patients with chronic myelogenous leukemia. The chromosome 22 breakpoint for this translocation is located within the BCR gene. The translocation produces a fusion protein which is encoded by sequence from both BCR and ABL, the gene at the chromosome 9 breakpoint. Although the BCR-ABL fusion protein has been extensively studied, the function of the normal BCR gene product is not clear. The protein has serine/threonine kinase activity and is a GTPase-activating protein for p21rac. Two transcript variants encoding different isoforms have been found for this gene.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6258R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6258R-CY3
Lokale Artikelnummer::
BOSSBS-6258R-CY3
Beschreibung:
A reciprocal translocation between chromosomes 22 and 9 produces the Philadelphia chromosome, which is often found in patients with chronic myelogenous leukemia. The chromosome 22 breakpoint for this translocation is located within the BCR gene. The translocation produces a fusion protein which is encoded by sequence from both BCR and ABL, the gene at the chromosome 9 breakpoint. Although the BCR-ABL fusion protein has been extensively studied, the function of the normal BCR gene product is not clear. The protein has serine/threonine kinase activity and is a GTPase-activating protein for p21rac. Two transcript variants encoding different isoforms have been found for this gene.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13747R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13747R-CY5
Lokale Artikelnummer::
BOSSBS-13747R-CY5
Beschreibung:
The claudin superfamily consists of many structurally related proteins that are important structural and functional components of tight junctions in paracellular transport. Claudins are located in both epithelial and endothelial cells in all tight junction-bearing tissues. Claudins, which consist of four transmembrane domains and two extracellular loops, make up tight junction strands. It is suggested that the claudin family of proteins regulate transport through tight junctions via differential discrimination for solute size and charge. Claudin expression is often highly restricted to specific regions of different tissues and may have an important role in transcellular transport through tight junctions. Claudin-22, also known as CLDN22, is a 220 amino acid member of the claudin family that participates in tight junction-specific obliteration of the intercellular space through calcium-independent cell-adhesion activity.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
8-Mercaptomenthone cis- und trans-Gemisch 97%
Artikel-Nr:
(BOSSBS-0235R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0235R-CY5.5
Lokale Artikelnummer::
BOSSBS-0235R-CY5.5
Beschreibung:
PMP22 is a 22 kDa glycoprotein expressed in the compact myelin of the peripheral nervous system. In the peripheral nervous system, PMP 22 is produced by myelinating Schwann cells and is coexpressed with the genes for myelin basic protein (MBP) during nerve development and regeneration. Alterations in the level of this protein cause several genetic human diseases. If the protein is duplicated, patients develop Charcot Marie Tooth disease. If one copy of the gene is deleted, they suffer from the inherited tendency to pressure palsies.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
(±)-β-Citronellol 95%
Lieferant:
Merck
Beschreibung:
Methylthymolblau Natriumsalz
Artikel-Nr:
(BOSSBS-1746R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1746R-HRP
Lokale Artikelnummer::
BOSSBS-1746R-HRP
Beschreibung:
This gene encodes the D4 subtype of the dopamine receptor. The D4 subtype is a G-protein coupled receptor which inhibits adenylyl cyclase. It is a target for drugs which treat schizophrenia and Parkinson disease. Mutations in this gene have been associated with various behavioral phenotypes, including autonomic nervous system dysfunction, attention deficit/hyperactivity disorder, and the personality trait of novelty seeking. This gene contains a polymorphic number (2-10 copies) of tandem 48 nt repeats; the sequence shown contains four repeats.DRD4 expression has been reported in various regions of the brain as well as in adrenal gland, artery, eye, heart, kidney, placenta, spinal cord, testis, and vas deferens.
VE:
1 * 100 µl
Lieferant:
ABEBA
Beschreibung:
Diese antistatischen Clogs aus Leder verfügen über einen klappbaren und verstellbaren Fersenriemen und eine Laufsohle aus Gummi mit Kreuz/Kreis-Profil. Die Sohle ist beständig gegen Säuren, Laugen (Reinigungsmittel) und Kraftstoffe.
Artikel-Nr:
(BOSSBS-15207R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15207R-A750
Lokale Artikelnummer::
BOSSBS-15207R-A750
Beschreibung:
C5orf48 (chromosome 5 open reading frame 48), also known as FLJ27505, MGC163367 or MGC163369, is a 134 amino acid protein. Encoded by a gene that maps to human chromosome 5q23.2, C5orf48 is linked to Autosomal dominant leukodystrophy (ADLD). Chromosome 5 makes up approximately 6% of the human genome and contains 181 million base pairs, which encode 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is caused by insertions or deletions within the TCOF1 gene and is also associated with chromosome 5. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15207R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15207R-HRP
Lokale Artikelnummer::
BOSSBS-15207R-HRP
Beschreibung:
C5orf48 (chromosome 5 open reading frame 48), also known as FLJ27505, MGC163367 or MGC163369, is a 134 amino acid protein. Encoded by a gene that maps to human chromosome 5q23.2, C5orf48 is linked to Autosomal dominant leukodystrophy (ADLD). Chromosome 5 makes up approximately 6% of the human genome and contains 181 million base pairs, which encode 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is caused by insertions or deletions within the TCOF1 gene and is also associated with chromosome 5. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1-Cyclopropyl-2,5-dimethyl-1H-pyrrole-3-carbaldehyde 95%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Methyl 2-nitro-4-(trifluoromethyl)benzoate 98%
Artikel-Nr:
(APOSOR931378-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR931378-5G
Lokale Artikelnummer::
APOSOR931378-5G
Beschreibung:
4-Isopropylcyclohexanecarboxylic acid (cis and trans mixture) 95%
VE:
1 * 5 g
Artikel-Nr:
(ACRO433440010)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
433440010
Lokale Artikelnummer::
ACRO433440010
Beschreibung:
4-Bromomethyl-2,6-dichloropyridine 97%
VE:
1 * 1 g
Preis auf Anfrage
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.
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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Dieses Produkt wurde von Ihrer Organisation gesperrt. Bitte kontaktieren Sie Ihren Einkauf für weitere Informationen.
Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
Dieses Produkt ist nicht mehr verfügbar. Bitte kontaktieren Sie den VWR Kundenservice.
|
|||||||||
Listenansicht
