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Artikel-Nr:
(BOSSBS-9728R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9728R-FITC
Lokale Artikelnummer::
BOSSBS-9728R-FITC
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-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9728R-A350
Lokale Artikelnummer::
BOSSBS-9728R-A350
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)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9728R
Lokale Artikelnummer::
BOSSBS-9728R
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:
(USBI0014-24D)
Lieferant:
US Biological
Hersteller-Artikelnummer::
0014-24D
Lokale Artikelnummer::
USBI0014-24D
Beschreibung:
Anti-14-3-3 delta/zeta Rabbit Polyclonal Antibody
VE:
1 * 50 µG
Lieferant:
Merck
Beschreibung:
Glycolsäure ≥70%, Sigma-Aldrich®
Lieferant:
Thermo Scientific
Beschreibung:
CAS No.: 2921-14-4
Lieferant:
Lenz Laborglas GmbH & CO.KG
Beschreibung:
DURAN®, borosilicate glass.
Lieferant:
Sigma-Aldrich
Beschreibung:
1,2,4-Trimethylbenzol, Sigma-Aldrich®
Artikel-Nr:
(1.09288.1000)
Lieferant:
Merck
Hersteller-Artikelnummer::
1.09288.1000
Lokale Artikelnummer::
MERC1.09288.1000
Beschreibung:
Kupfer(II)-ethylendiamin 1 mol/l (3 N) in wässriger Lösung für die Viskositätsmessung von Cellulose gemäß DIN 54270, Supelco®
VE:
1 * 1 L
Lieferant:
Sigma-Aldrich
Beschreibung:
α-Methylstyrol, Sigma-Aldrich®
Lieferant:
COMBI-BLOCKS
Beschreibung:
1,3-Dibrom-5-tert-butylbenzol
Lieferant:
SIGMA ALDRICH MICROSCOPY
Beschreibung:
Methylenblau ≥82% (Farbstoffgehalt), zertifiziert durch die Biological Stain Commission, Sigma-Aldrich®
Lieferant:
Bernd Kraft
Beschreibung:
Cyclohexan, technische Qualität
Artikel-Nr:
(SIAL235806-100G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
235806-100G
Lokale Artikelnummer::
SIAL235806-100G
Beschreibung:
3,4-Dichlor-α,α,α-trifluortoluol, Sigma-Aldrich®
VE:
1 * 100 g
Artikel-Nr:
(212-0748)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRI212-0748
Beschreibung:
Test tubes made from borosilicate 7.1 glass, ideal for use as disposable.
VE:
1 * 1.000 ST
Artikel-Nr:
(34140.184)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC34140.184
Beschreibung:
Kongorot, TECHNICAL
VE:
1 * 100 g
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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