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Product Image-731-0139

Systémy pro purifikaci nukleových kyselin a proteinů, KingFisher™ Flex

Dodavatel: Thermo Fisher Scientific
Popis: Procesory magnetických částic KingFisher™ jsou navrženy tak, aby automatizovaly časově náročné zpracování vzorků nukleových kyselin, proteinů nebo buněk prakticky z jakéhokoli zdroje (například z krve, buněčných kultur, tkáňových lyzátů, půdy nebo výkalů). Řada KingFisher™ se skládá z přístrojů s různou výkonností a objemovou kapacitou, které splňují individuální potřeby zpracování vzorků. Každý systém se skládá z přístroje, speciálně navržených plastových potřeb a softwaru. Systémy KingFisher™ se postarají o rychlou a reprodukovatelnou purifikaci vysoce kvalitní DNA, RNA, proteinů a buněk v nejrůznějších aplikacích od genomiky a proteomiky přes výzkum a vývoj léčiv, forenzní metody, výzkum biomarkerů, kontroly kvality až po veterinární testy.

Image Unavailable-EHERC11940000

Kyselina (2,4-Dichlorfenoxy)octová

Katalogové číslo: (EHERC11940000)
Dodavatel: EHRENSTORFER
Popis: Kyselina (2,4-Dichlorfenoxy)octová
Měrná jednotka: 1 * 0,25 g

Certifikáty


Image Unavailable-SIALM42505-100G

Methyl-2,4-dihydroxybenzoate, Sigma-Aldrich®

Dodavatel: Merck
Popis: Methyl-2,4-dihydroxybenzoate, Sigma-Aldrich®

Product Image-ACRO229650250

Eozin B, high purity biological stain

Dodavatel: Thermo Fisher Scientific
Popis: Eozin B, high purity biological stain

Bezpečnostní list

Product Image-ACRO409420250

Eozin B, pure, certified

Dodavatel: Thermo Fisher Scientific
Popis: Eozin B, pure, certified

Bezpečnostní list

Image Unavailable-PROOBP706

Ursodeoxycholic acid

Katalogové číslo: (PROOBP706)
Dodavatel: LGC Standards PROMOCHEM
Popis: Ursodeoxycholic acid
Měrná jednotka: 1 * 150 mg
Image Unavailable-BOSSBS-13315R-A750

Anti-Gcn1l1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Katalogové číslo: (BOSSBS-13315R-A750)
Dodavatel: Bioss
Popis: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-13315R

Anti-GCN1 Rabbit Polyclonal Antibody

Katalogové číslo: (BOSSBS-13315R)
Dodavatel: Bioss
Popis: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-13315R-HRP

Anti-GCN1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Katalogové číslo: (BOSSBS-13315R-HRP)
Dodavatel: Bioss
Popis: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-13315R-CY3

Anti-GCN1 Rabbit Polyclonal Antibody (Cy3®)

Katalogové číslo: (BOSSBS-13315R-CY3)
Dodavatel: Bioss
Popis: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-13315R-A555

Anti-GCN1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Katalogové číslo: (BOSSBS-13315R-A555)
Dodavatel: Bioss
Popis: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-13315R-FITC

Anti-GCN1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Katalogové číslo: (BOSSBS-13315R-FITC)
Dodavatel: Bioss
Popis: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-13315R-A647

Anti-GCN1 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Katalogové číslo: (BOSSBS-13315R-A647)
Dodavatel: Bioss
Popis: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-13315R-A350

Anti-GCN1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Katalogové číslo: (BOSSBS-13315R-A350)
Dodavatel: Bioss
Popis: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Měrná jednotka: 1 * 100 µl
Image Unavailable-SIALC9377-5G

Chenodeoxycholic acid, Sigma-Aldrich®

Dodavatel: Merck
Popis: Chenodeoxycholic acid, Sigma-Aldrich®

Image Unavailable-BOSSBS-13315R-A488

Anti-GCN1 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Katalogové číslo: (BOSSBS-13315R-A488)
Dodavatel: Bioss
Popis: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Měrná jednotka: 1 * 100 µl
Cena na vyžádání
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Omezené množství produktu na skladě. Zboží může být k dispozici v jiném skladě poblíž vašeho sídla. Přesvědčte se, že jste přihlášení na stránky, abyste mohli vidět dostupné položky na skladě. Pokud je stále zobrazeno call a potřebujete asistenci, volejte na číslo 321 570 321.
Daná chemikálie je regulována dle platné legislativy a bude vyžadováno vyplnění formuláře. Jeho včasným vyplněním uspíšíte dodání produktu.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Tento produkt je zablokován vaší organizací. Kontaktujte své nákupní oddělení pro více informací.
Původní produkt již není k dispozici. Zobrazen je náhradní produkt.
Tento produkt již není k dispozici. Podobné produkty můžete vyhledat pomocí VWR katalogových čísel nebo čísel dodavatele uvedených výše. Pokud potřebujete další asistenci, zavolejte na telefonní číslo zákaznického servisu VWR 321 570 321.
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