1,4-Diazabicyclo[2.2.2]octanebis(sulphur+dioxide)adduct
Artikel-Nr:
(D-047-1ML)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
D-047-1ML
Lokale Artikelnummer::
SUPLD-047-1ML
Beschreibung:
Organic Standard, N-Desmethylcitalopram hydrochloride solution, ampoule of 1 ml
VE:
1 * 1 mL
Artikel-Nr:
(USBIM2352-03U-APC)
Lieferant:
US Biological
Hersteller-Artikelnummer::
M2352-03U-APC
Lokale Artikelnummer::
USBIM2352-03U-APC
Beschreibung:
Anti-MAP Kinase 14 Rabbit Polyclonal Antibody (APC (Allophycocyanin))
VE:
1 * 200 µl
Lieferant:
Lenz Laborglas GmbH & CO.KG
Beschreibung:
DURAN®, Borosilikatglas, klar.
Lieferant:
Merck
Beschreibung:
Natriumdithionit, EMPLURA®, Supelco®
Lieferant:
Bohlender
Beschreibung:
Sicherungsscheibe, BOLA, Für: NS 29,2, Unterlegscheiben, PTFE, Kegel 1:10, Gewinde M 14
Artikel-Nr:
(BLDPBD01119606-50M)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD01119606-50M
Lokale Artikelnummer::
BLDPBD01119606-50M
Beschreibung:
DMNQ 99%
VE:
1 * 50 mg
Artikel-Nr:
(8.20044.0010)
Lieferant:
Merck
Hersteller-Artikelnummer::
8.20044.0010
Lokale Artikelnummer::
MERC8.20044.0010
Beschreibung:
o-Ethyltoluol zur Synthese, Sigma-Aldrich®
VE:
1 * 10 mL
Artikel-Nr:
(ABCAAB243232-1ML)
Lieferant:
Abcam
Beschreibung:
Anti-VEGF Receptor 3 Rabbit Monoclonal Antibody [clone: EPR22293-14]
VE:
1 * 1 mL
New Product
Lieferant:
Spectrum Chemical
Beschreibung:
Magnesium Sulfate, Heptahydrate, FCC, commonly called Epsom salt, is used as a brewing salt in beer production and a tofu coagulant. The FCC grade meets the requirements of the Food Chemical Codex indicates and is suitable for all food, beverage and nutritional supplement applications. Spectrum Chemical offers over 300 Food grade chemical ingredients packaged in laboratory size bottles to production drum quantities and are manufactured, packaged and stored under current Good Manufacturing Practices (cGMP) per 21CFR part 211 in FDA registered and inspected facilities.
Artikel-Nr:
(19531-25MG)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
19531-25MG
Lokale Artikelnummer::
SUPL19531-25MG
Beschreibung:
Organic Standard, Sudan Blue II, ≥98.0% (HPLC)
VE:
1 * 25 mg
Artikel-Nr:
(BOSSBS-9728R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9728R-A555
Lokale Artikelnummer::
BOSSBS-9728R-A555
Beschreibung:
β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a β-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9728R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9728R-A647
Lokale Artikelnummer::
BOSSBS-9728R-A647
Beschreibung:
β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a β-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9728R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9728R-CY5
Lokale Artikelnummer::
BOSSBS-9728R-CY5
Beschreibung:
β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a β-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar.
VE:
1 * 100 µl
Artikel-Nr:
(232-0053)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRI232-0053
Beschreibung:
PTFE, mit Stahlfederkern. Sehr stabil, sicher und langlebig, einfache Handhabung.
VE:
1 * 1 ST
Preis auf Anfrage
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