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Proguanil+hydrochloride


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Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-4037R-CY3
Lokale Artikelnummer:: BOSSBS-4037R-CY3
Beschreibung:   SLC25A11 catalyzes the transport of 2-oxoglutarate across the inner mitochondrial membrane in an electroneutral exchange for malate or other dicarboxylic acids, and plays an important role in several metabolic processes, including the malate-aspartate shuttle, the oxoglutarate/isocitrate shuttle, in gluconeogenesis from lactate, and in nitrogen metabolism.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8518R-A488
Lokale Artikelnummer:: BOSSBS-8518R-A488
Beschreibung:   SPP24, also known as secreted phosphoprotein 2, is a 211 amino acid secreted protein that belongs to the cystatin superfamily. Expressed in liver and plasma, SPP24 may play a role in coordinating an aspect of bone turnover. The gene that encodes SPP24 maps to human chromosome 2, which consists of 237 million bases encoding over 1,400 genes, making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
VE:  1 * 100 µl
Lieferant:  Honeywell Chemicals
Hersteller-Artikelnummer:: 34493-2.5L
Lokale Artikelnummer:: HONC34493-2.5L
Beschreibung:   Hexan (Isomerengemisch), CHROMASOLV™ für die Analyse von Pestizidrückständen, Riedel-de Haën™
VE:  1 * 2,5 L
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8518R-FITC
Lokale Artikelnummer:: BOSSBS-8518R-FITC
Beschreibung:   SPP24, also known as secreted phosphoprotein 2, is a 211 amino acid secreted protein that belongs to the cystatin superfamily. Expressed in liver and plasma, SPP24 may play a role in coordinating an aspect of bone turnover. The gene that encodes SPP24 maps to human chromosome 2, which consists of 237 million bases encoding over 1,400 genes, making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
VE:  1 * 100 µl
Lieferant:  BLD PHARMATECH GMBH
Hersteller-Artikelnummer:: BD42078-5G
Lokale Artikelnummer:: BLDPBD42078-5G
Beschreibung:   N-(tert-Butoxycarbonyl)-trans-4-(p-toluenesulphonyloxy)-L-proline methyl ester 95%
VE:  1 * 5 g
Lieferant:  BIOLEGEND INC
Hersteller-Artikelnummer:: 141102
Lokale Artikelnummer:: BLEG141102
Beschreibung:   Anti-TCRG Armenian Hamster Monoclonal Antibody [clone: 2.11]
VE:  1 * 100 µG
Market Source Item This is a MarketSource item. Additional charges may apply
Lieferant:  Honeywell Chemicals
Beschreibung:   ACS GENERAL USE SOLVENTS
Lieferant:  Honeywell Chemicals
Beschreibung:   n-Hexan für die Gaschromatographie, Burdick & Jackson™

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8518R-A350
Lokale Artikelnummer:: BOSSBS-8518R-A350
Beschreibung:   SPP24, also known as secreted phosphoprotein 2, is a 211 amino acid secreted protein that belongs to the cystatin superfamily. Expressed in liver and plasma, SPP24 may play a role in coordinating an aspect of bone turnover. The gene that encodes SPP24 maps to human chromosome 2, which consists of 237 million bases encoding over 1,400 genes, making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-4037R-CY5
Lokale Artikelnummer:: BOSSBS-4037R-CY5
Beschreibung:   SLC25A11 catalyzes the transport of 2-oxoglutarate across the inner mitochondrial membrane in an electroneutral exchange for malate or other dicarboxylic acids, and plays an important role in several metabolic processes, including the malate-aspartate shuttle, the oxoglutarate/isocitrate shuttle, in gluconeogenesis from lactate, and in nitrogen metabolism.
VE:  1 * 100 µl

Lieferant:  Merck
Hersteller-Artikelnummer:: ZIQELEMT0
Lokale Artikelnummer:: MILLZIQELEMT0
Beschreibung:   Milli-Q® IQ Element water purification and dispensing unit is designed to fit into your trace analysis workflow. The Milli-Q® IQ Element unit, combined with a Milli-Q® IQ 7 series water purification system, delivers analytical grade ultrapure water that is suitable for trace and ultra-trace elemental analyses, including ICP-MS, GF-AAS and trace IC.
VE:  1 * 1 ST
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-4037R-HRP
Lokale Artikelnummer:: BOSSBS-4037R-HRP
Beschreibung:   SLC25A11 catalyzes the transport of 2-oxoglutarate across the inner mitochondrial membrane in an electroneutral exchange for malate or other dicarboxylic acids, and plays an important role in several metabolic processes, including the malate-aspartate shuttle, the oxoglutarate/isocitrate shuttle, in gluconeogenesis from lactate, and in nitrogen metabolism.
VE:  1 * 100 µl
Lieferant:  Honeywell Chemicals
Beschreibung:   n-Hexan ≥95% (durch GC), CHROMASOLV™ für die Analyse von Pestizidrückständen, zur Analyse von Dioxinen, Furan und PCB, Riedel-de Haën™
Artikel-Nr: (BOSSBS-11944R-CY5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11944R-CY5
Lokale Artikelnummer:: BOSSBS-11944R-CY5
Beschreibung:   RILPL2 is a 211 amino acid protein that belongs to the RILPL family. RILPL2 does not regulate lysosomal morphology or distribution. RILPL2 shares 32% and 18% amino acid identity with RILPL1 and RILP, respectively. RILPL2 as a novel interacting partner for the actin-based molecular motor MyoVa, and has a novel role for RILPL2 in controlling neuronal morphogenesis. It has been suggested that there is also a novel role for RILPL2 in the regulation of cellular shape and dendritic-spine morphogenesis, probably via the Rac1-Pak pathway. PCR analysis of human tissues detects highest RILPL2 expression in lung, followed by placenta. Lower expression is detected in liver, kidney, pancreas, heart and brain, but no expression is detected in skeletal muscle. The RILPL2 gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 12q24.31.
VE:  1 * 100 µl
Lieferant:  KARTELL
Beschreibung:   Konisch zulaufende Stopfen, PTFE, plastilab®, NS: 24/29, Ø unten: 21,1 mm
Lieferant:  Bernd Kraft
Hersteller-Artikelnummer:: 12510.4700
Lokale Artikelnummer:: KRAF12510.4700
Beschreibung:   n-Hexan, isokratische Qualität für die HPLC, für die Spektroskopie
VE:  1 * 2,5 L
Preis auf Anfrage
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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 call noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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