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[1-(3-Methylpyridin-2-yl)propyl]amine
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[1-(3-Methylpyridin-2-yl)propyl]amine
Lieferant:
Bertin Instruments
Beschreibung:
The Precellys lysing kits offer the best versatility of volumes and grinding material to process any type of samples: Human, animal, plants, microorganisms or soil.
Lieferant:
Alfa Aesar
Beschreibung:
2-tert-Butylhydrochinon ≥97%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Dihydrocytochalasin B
Artikel-Nr:
(BOSSBS-8260R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8260R-CY3
Lokale Artikelnummer::
BOSSBS-8260R-CY3
Beschreibung:
DHRS1 (dehydrogenase/reductase (SDR family) member 1), also known as SDR19C1, is a 313 amino acid protein that belongs to the short-chain dehydrogenases/reductases (SDR) family and likely functions as an oxidoreductase. Abundantly expressed in heart and liver, DHRS1 contains an SDR motif and is encoded by a gene that maps to human chromosome 14q12. Human chromosome 14 houses over 700 genes and comprises nearly 3.5% of the human genome. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD). The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder ?-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.
VE:
1 * 100 µl
Artikel-Nr:
(70-0621-U100)
Lieferant:
Tonbo Biosciences
Hersteller-Artikelnummer::
70-0621-U100
Lokale Artikelnummer::
TNBO70-0621-U100
Beschreibung:
The MEL-14 antibody is specific for mouse CD62L, also known as L-Selectin, a cell adhesion molecule which facilitates lymphocyte “rolling” on activated vascular endothelium and homing to high endothelial venules (HEV) as immune cells transmigrate from blood into peripheral tissues. L-Selectin is a member of a family of Selectin molecules which act together with the integrin family of adhesion molecules to mediate leukocyte-endothelial interactions. L-Selectin is characteristically expressed by neutrophils, and is also found on B cells, monocytes, granulocytes, and at varying levels on naive, effector and memory T cells. It is rapidly shed upon cell activation, releasing into the circulation a soluble form whose biological role is of particular interest in cancer biology research.
VE:
1 * 100 µG
Artikel-Nr:
(BOSSBS-8260R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8260R-CY7
Lokale Artikelnummer::
BOSSBS-8260R-CY7
Beschreibung:
DHRS1 (dehydrogenase/reductase (SDR family) member 1), also known as SDR19C1, is a 313 amino acid protein that belongs to the short-chain dehydrogenases/reductases (SDR) family and likely functions as an oxidoreductase. Abundantly expressed in heart and liver, DHRS1 contains an SDR motif and is encoded by a gene that maps to human chromosome 14q12. Human chromosome 14 houses over 700 genes and comprises nearly 3.5% of the human genome. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD). The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder ?-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.
VE:
1 * 100 µl
Artikel-Nr:
(VWRS6039.5000)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRS6039.5000
Beschreibung:
Natriumchlorid 26% in wässriger Lösung
VE:
1 * 5 L
Lieferant:
Brand
Beschreibung:
Borosilikatglas 3.3, mit PP-Stopfen.
Lieferant:
HIRSCHMANN
Beschreibung:
Einmalkapillaren für das Zentrifugieren von Blutproben.
Artikel-Nr:
(BOSSBS-9741R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9741R-CY3
Lokale Artikelnummer::
BOSSBS-9741R-CY3
Beschreibung:
ANGEL1 , also known as KIAA0759, is a 670 amino acid protein belonging to the CKR-4 protein family. ANGEL1 is encoded by a gene located on human chromosome 14, which contains about 700 genes and 106 million base pairs, making up about 3.5% of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and, when defective, leads to the genetic disorder ?-antitrypsin deficiency. This disorder is characterized by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus on chromosome 14 and its fusion via translocation with the chromosome 19 encoded protein BCL3 may be related to B-cell malignancies.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
Nitroterephthalsäure ≥99%
Artikel-Nr:
(1.09945.0001)
Lieferant:
Merck
Hersteller-Artikelnummer::
1.09945.0001
Lokale Artikelnummer::
MERC1.09945.0001
Beschreibung:
Natriumchlorid 0.1 mol/l konzentrierte wässrige Lösung, Titrisol®, Supelco®
VE:
1 * 1 Ampull
Artikel-Nr:
(NALG642015-2800)
Lieferant:
Thermo Fisher Scientific
Hersteller-Artikelnummer::
642015-2800
Lokale Artikelnummer::
NALG642015-2800
Beschreibung:
Square shaped media bottles.
VE:
1 * 96 ST
Artikel-Nr:
(PRSI30-101)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
30-101
Lokale Artikelnummer::
PRSI30-101
Beschreibung:
ECHS1 functions in the second step of the mitochondrial fatty acid beta-oxidation pathway. It catalyzes the hydration of 2-trans-enoyl-coenzyme A (CoA) intermediates to L-3-hydroxyacyl-CoAs. ECHS1 is a member of the hydratase/isomerase superfamily. It localizes to the mitochondrial matrix.The protein encoded by this gene functions in the second step of the mitochondrial fatty acid beta-oxidation pathway. It catalyzes the hydration of 2-trans-enoyl-coenzyme A (CoA) intermediates to L-3-hydroxyacyl-CoAs. The gene product is a member of the hydratase/isomerase superfamily. It localizes to the mitochondrial matrix. Transcript variants utilizing alternative transcription initiation sites have been described in the literature.
VE:
1 * 100 µG
Artikel-Nr:
(PRSI26-725)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
26-725
Lokale Artikelnummer::
PRSI26-725
Beschreibung:
RDH12 is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. RDH12 also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 3 (LCA3).The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 3 (LCA3).
VE:
1 * 50 µG
Lieferant:
DWK Life Sciences
Beschreibung:
Kalk-Soda-Glas mit geradem Rand.
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.
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