Suche >
3-(Trifluormethylthio)benzonitril
Drucken
Sie suchten nach:
0 results were found
3-(Trifluormethylthio)benzonitril
Lieferant:
Sigma-Aldrich
Beschreibung:
D(+)-Trehalose Dihydrat, Millipore®
Artikel-Nr:
(BOSSBS-0964R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0964R-CY5
Lokale Artikelnummer::
BOSSBS-0964R-CY5
Beschreibung:
Tripartite motif-containing protein 32 (TRIM32) belongs to the tripartite motif (TRIM) protein family. TRIM32, like all TRIM proteins, contains a domain structure composed of a B-box, a RING-finger and a coiled-coil motif. Additionally, TRIM32 has six C-terminal NHL domains; it is expressed mainly in the skeletal muscle. The TRIM32 gene encodes an E3 ubiquitin ligase, a protein that attaches ubiquitin to a lysine residue on a target protein and acts in conjunction with ubiquitin-conjugating enzymes UbcH5a, UbcH5c and UbcH6. Mutations in the TRIM32 gene cause two forms of autosomal recessive muscular dystrophy designated limb girdle muscular dystrophy type 2H (LGMD2H) and sarcotubular myopathy (STM). TRIM32 mutations can also result in Bardet-Biedl syndrome (BBS), an autosomal recessive disorder characterized by pigmentary retinopathy, polydactyly, hypogenitalism, renal abnormalities, learning disabilities and obesity.
VE:
1 * 100 µl
Artikel-Nr:
(SERA39551.01)
Lieferant:
Serva
Hersteller-Artikelnummer::
39551.01
Lokale Artikelnummer::
SERA39551.01
Beschreibung:
Calciumchlorid Dihydrat
VE:
1 * 250 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(SERA15587.02)
Lieferant:
Serva
Hersteller-Artikelnummer::
15587.02
Lokale Artikelnummer::
SERA15587.02
Beschreibung:
Calciumchlorid Dihydrat
VE:
1 * 1 kg
This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(MOLEM31244850)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M31244850
Lokale Artikelnummer::
MOLEM31244850
Beschreibung:
Riboflavin-5'-phosphat Natriumsalz Dihydrat
VE:
1 * 10 g
This is a MarketSource item. Additional charges may apply
Lieferant:
Thermo Scientific
Beschreibung:
EDTA Dinatriumsalz Dihydrat 99+% für die Molekularbiologie DNAse-, RNAse-, proteasefrei
Lieferant:
Sigma-Aldrich
Beschreibung:
D(+)-Trehalose Dihydrat, Sigma-Aldrich®
Artikel-Nr:
(SIALF1392-25MG)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
F1392-25MG
Lokale Artikelnummer::
SIALF1392-25MG
Beschreibung:
Riboflavin-5'-phosphat Natriumsalz Dihydrat, Sigma-Aldrich®
VE:
1 * 25 mg
Lieferant:
Sigma-Aldrich
Beschreibung:
D(+)-Trehalose Dihydrat, Sigma-Aldrich®
Artikel-Nr:
(MOLEM28499276)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M28499276
Lokale Artikelnummer::
MOLEM28499276
Beschreibung:
3-Methylxanthin
VE:
1 * 100 mg
This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-0964R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0964R-A350
Lokale Artikelnummer::
BOSSBS-0964R-A350
Beschreibung:
Tripartite motif-containing protein 32 (TRIM32) belongs to the tripartite motif (TRIM) protein family. TRIM32, like all TRIM proteins, contains a domain structure composed of a B-box, a RING-finger and a coiled-coil motif. Additionally, TRIM32 has six C-terminal NHL domains; it is expressed mainly in the skeletal muscle. The TRIM32 gene encodes an E3 ubiquitin ligase, a protein that attaches ubiquitin to a lysine residue on a target protein and acts in conjunction with ubiquitin-conjugating enzymes UbcH5a, UbcH5c and UbcH6. Mutations in the TRIM32 gene cause two forms of autosomal recessive muscular dystrophy designated limb girdle muscular dystrophy type 2H (LGMD2H) and sarcotubular myopathy (STM). TRIM32 mutations can also result in Bardet-Biedl syndrome (BBS), an autosomal recessive disorder characterized by pigmentary retinopathy, polydactyly, hypogenitalism, renal abnormalities, learning disabilities and obesity.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0964R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0964R-A680
Lokale Artikelnummer::
BOSSBS-0964R-A680
Beschreibung:
Tripartite motif-containing protein 32 (TRIM32) belongs to the tripartite motif (TRIM) protein family. TRIM32, like all TRIM proteins, contains a domain structure composed of a B-box, a RING-finger and a coiled-coil motif. Additionally, TRIM32 has six C-terminal NHL domains; it is expressed mainly in the skeletal muscle. The TRIM32 gene encodes an E3 ubiquitin ligase, a protein that attaches ubiquitin to a lysine residue on a target protein and acts in conjunction with ubiquitin-conjugating enzymes UbcH5a, UbcH5c and UbcH6. Mutations in the TRIM32 gene cause two forms of autosomal recessive muscular dystrophy designated limb girdle muscular dystrophy type 2H (LGMD2H) and sarcotubular myopathy (STM). TRIM32 mutations can also result in Bardet-Biedl syndrome (BBS), an autosomal recessive disorder characterised by pigmentary retinopathy, polydactyly, hypogenitalism, renal abnormalities, learning disabilities and obesity.
VE:
1 * 100 µl
Artikel-Nr:
(EHERC17607500)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C17607500
Lokale Artikelnummer::
EHERC17607500
Beschreibung:
D(+)-Trehalose Dihydrat
VE:
1 * 0,25 g
Artikel-Nr:
(BOSSBS-0964R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0964R-A750
Lokale Artikelnummer::
BOSSBS-0964R-A750
Beschreibung:
Tripartite motif-containing protein 32 (TRIM32) belongs to the tripartite motif (TRIM) protein family. TRIM32, like all TRIM proteins, contains a domain structure composed of a B-box, a RING-finger and a coiled-coil motif. Additionally, TRIM32 has six C-terminal NHL domains; it is expressed mainly in the skeletal muscle. The TRIM32 gene encodes an E3 ubiquitin ligase, a protein that attaches ubiquitin to a lysine residue on a target protein and acts in conjunction with ubiquitin-conjugating enzymes UbcH5a, UbcH5c and UbcH6. Mutations in the TRIM32 gene cause two forms of autosomal recessive muscular dystrophy designated limb girdle muscular dystrophy type 2H (LGMD2H) and sarcotubular myopathy (STM). TRIM32 mutations can also result in Bardet-Biedl syndrome (BBS), an autosomal recessive disorder characterized by pigmentary retinopathy, polydactyly, hypogenitalism, renal abnormalities, learning disabilities and obesity.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0964R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0964R-CY7
Lokale Artikelnummer::
BOSSBS-0964R-CY7
Beschreibung:
Tripartite motif-containing protein 32 (TRIM32) belongs to the tripartite motif (TRIM) protein family. TRIM32, like all TRIM proteins, contains a domain structure composed of a B-box, a RING-finger and a coiled-coil motif. Additionally, TRIM32 has six C-terminal NHL domains; it is expressed mainly in the skeletal muscle. The TRIM32 gene encodes an E3 ubiquitin ligase, a protein that attaches ubiquitin to a lysine residue on a target protein and acts in conjunction with ubiquitin-conjugating enzymes UbcH5a, UbcH5c and UbcH6. Mutations in the TRIM32 gene cause two forms of autosomal recessive muscular dystrophy designated limb girdle muscular dystrophy type 2H (LGMD2H) and sarcotubular myopathy (STM). TRIM32 mutations can also result in Bardet-Biedl syndrome (BBS), an autosomal recessive disorder characterized by pigmentary retinopathy, polydactyly, hypogenitalism, renal abnormalities, learning disabilities and obesity.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0964R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0964R
Lokale Artikelnummer::
BOSSBS-0964R
Beschreibung:
Tripartite motif-containing protein 32 (TRIM32) belongs to the tripartite motif (TRIM) protein family. TRIM32, like all TRIM proteins, contains a domain structure composed of a B-box, a RING-finger and a coiled-coil motif. Additionally, TRIM32 has six C-terminal NHL domains; it is expressed mainly in the skeletal muscle. The TRIM32 gene encodes an E3 ubiquitin ligase, a protein that attaches ubiquitin to a lysine residue on a target protein and acts in conjunction with ubiquitin-conjugating enzymes UbcH5a, UbcH5c and UbcH6. Mutations in the TRIM32 gene cause two forms of autosomal recessive muscular dystrophy designated limb girdle muscular dystrophy type 2H (LGMD2H) and sarcotubular myopathy (STM). TRIM32 mutations can also result in Bardet-Biedl syndrome (BBS), an autosomal recessive disorder characterized by pigmentary retinopathy, polydactyly, hypogenitalism, renal abnormalities, learning disabilities and obesity.
VE:
1 * 100 µl
Preis auf Anfrage
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.
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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Dieses Produkt wurde von Ihrer Organisation gesperrt. Bitte kontaktieren Sie Ihren Einkauf für weitere Informationen.
Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
Dieses Produkt ist nicht mehr verfügbar. Bitte kontaktieren Sie den VWR Kundenservice.
|
|||||||||
Listenansicht
