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Artikel-Nr:
(BOSSBS-8518R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8518R-A680
Lokale Artikelnummer::
BOSSBS-8518R-A680
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, Alstr 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:
Thermo Scientific
Beschreibung:
n-Hexan 97+% ACS, erfüllt analytische Spezifikationen von Reagent Ph. Eur. für die HPLC
Lieferant:
Thermo Scientific
Beschreibung:
n-Hexan, extra trocken über Molekularsieb 97%, AcroSeal®
Lieferant:
Thermo Scientific
Beschreibung:
Hexan (Isomerengemisch), extra trocken 99.9%, AcroSeal®
Artikel-Nr:
(CAYM21572-100)
Lieferant:
Cayman Chemical
Hersteller-Artikelnummer::
21572-100
Lokale Artikelnummer::
CAYM21572-100
Beschreibung:
β-Caryophyllene is a sesquiterpene that has been found in plants, including C. sativa, C. indica, and hemp, and has diverse biological activities, including lipid metabolic, antioxidant, anti-neuroinflammatory, anti-proliferative, and antinociceptive properties.
VE:
1 * 100 mg
Artikel-Nr:
(BOSSBS-4037R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4037R-A750
Lokale Artikelnummer::
BOSSBS-4037R-A750
Beschreibung:
SLC25A11 catalyses 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
Artikel-Nr:
(BOSSBS-4037R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4037R-A680
Lokale Artikelnummer::
BOSSBS-4037R-A680
Beschreibung:
SLC25A11 catalyses 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
Artikel-Nr:
(BOSSBS-8518R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8518R-A647
Lokale Artikelnummer::
BOSSBS-8518R-A647
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
Artikel-Nr:
(BOSSBS-8518R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8518R-HRP
Lokale Artikelnummer::
BOSSBS-8518R-HRP
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
Artikel-Nr:
(BOSSBS-8518R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8518R-A555
Lokale Artikelnummer::
BOSSBS-8518R-A555
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
Artikel-Nr:
(EHERC14195500)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C14195500
Lokale Artikelnummer::
EHERC14195500
Beschreibung:
n-Hexan zertifiziertes Referenzmaterial (ISO 17034)
VE:
1 * 1 mL
Artikel-Nr:
(BOSSBS-8518R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8518R-A750
Lokale Artikelnummer::
BOSSBS-8518R-A750
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, Alstr 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
Artikel-Nr:
(BOSSBS-4037R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4037R-CY7
Lokale Artikelnummer::
BOSSBS-4037R-CY7
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
Artikel-Nr:
(BOSSBS-4037R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4037R-CY5.5
Lokale Artikelnummer::
BOSSBS-4037R-CY5.5
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
Artikel-Nr:
(34493-2.5L)
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
Artikel-Nr:
(BOSSBS-4037R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4037R-A647
Lokale Artikelnummer::
BOSSBS-4037R-A647
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
Preis auf Anfrage
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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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