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HEPES, powder cell culture reagent, not sterile

Dodavatel: Biowest
Popis: HEPES, powder cell culture reagent, not sterile

Bezpečnostní list Certifikáty

Image Unavailable-APOSBI8181-100G

HEPES free acid ≥99.5%, Ultrapure

Dodavatel: Apollo Scientific
Popis: Biological buffer - useful range 6.8 - 8.2

Image Unavailable-BOSSBS-8319R-A555

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

Katalogové číslo: (BOSSBS-8319R-A555)
Dodavatel: Bioss
Popis: LHPP, also known as HDHD2B, is a 270 amino acid protein that exists as a homodimer and is a member of the HAD-like hydrolase superfamily. Expressed in liver, kidney and moderately in brain, LHPP is encoded by a gene located on 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
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
Product Image-A1069.5000

HEPES ≥99.5% suitable for buffer solutions

Dodavatel: PanReac AppliChem
Popis: HEPES ≥99.5% suitable for buffer solutions

Product Image-441476L

HEPES ≥99.5%

Katalogové číslo: (441476L)
Dodavatel: VWR Chemicals
Popis: Hepes is a widely used buffer in biological studies. In cell culture media, it is employed as a substitute for the bicarbonate buffer at a concentration of 25 mM or as a supplement to the bicarbonate buffer (concentration 10 to 15 mM).
Měrná jednotka: 1 * 1 kg

Bezpečnostní list Certifikáty


Image Unavailable-APOSBIV0155-5G

Vancomycin hydrochloride

Dodavatel: Apollo Scientific
Popis: Vancomycin is a glycopeptide antibiotic. It exerts its action by inhibiting the formation of the peptidoglycan polymers of the bacterial cell wall. Often used incombination with cefotaxim or carbenicillin.

Product Image-ACRO410570050

Ferrozine mono-sodium salt hydrate 98+%, pure

Dodavatel: Thermo Fisher Scientific
Popis: FerroZine™ iron reagent

Bezpečnostní list

Image Unavailable-APOSOR911625-25G

tert-Butyl-5-norbornene-2-carboxylate (endo and exo mixture) 95%

Dodavatel: Apollo Scientific
Popis: tert-Butyl-5-norbornene-2-carboxylate (endo and exo mixture) 95%

Image Unavailable-BOSSBS-8319R-CY3

Anti-LHPP Rabbit Polyclonal Antibody (Cy3®)

Katalogové číslo: (BOSSBS-8319R-CY3)
Dodavatel: Bioss
Popis: LHPP, also known as HDHD2B, is a 270 amino acid protein that exists as a homodimer and is a member of the HAD-like hydrolase superfamily. Expressed in liver, kidney and moderately in brain, LHPP is encoded by a gene located on 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-8319R-CY7

Anti-LHPP Rabbit Polyclonal Antibody (Cy7®)

Katalogové číslo: (BOSSBS-8319R-CY7)
Dodavatel: Bioss
Popis: LHPP, also known as HDHD2B, is a 270 amino acid protein that exists as a homodimer and is a member of the HAD-like hydrolase superfamily. Expressed in liver, kidney and moderately in brain, LHPP is encoded by a gene located on 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Měrná jednotka: 1 * 100 µl
Image Unavailable-BOSSBS-13315R-A680

Anti-Gcn1l1 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Katalogové číslo: (BOSSBS-13315R-A680)
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-CY5

Anti-GCN1 Rabbit Polyclonal Antibody (Cy5®)

Katalogové číslo: (BOSSBS-13315R-CY5)
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-CY7

Anti-GCN1 Rabbit Polyclonal Antibody (Cy7®)

Katalogové číslo: (BOSSBS-13315R-CY7)
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
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.
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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