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Beschreibung: Advanced airflow technology makes this the most energy efficient compressed air filtration system available.
Artikel-Nr: MFLX29587-11
UOM: 1 * 1 ST
Hersteller Artikel Nummer : 29587-11
Lieferant: Avantor Fluid Handling


Beschreibung: Die Wasserstoffgeneratoren von Parker Domnick Hunter erzeugen einen kontinuierlichen Fluss hochreinen Wasserstoffs aus entionisiertem Wasser. Diese Wasserstoffgeneratoren sind eine sichere und bedienungsfreundliche Alternative zu Hochdruckgaszylindern. Wasserstoff wird nur nach Bedarf bei niedrigem Druck erzeugt, und das Volumen des gespeicherten Gases ist minimal.
Artikel-Nr: DHUN110H-MDCARRIER
UOM: 1 * 1 ST
Hersteller Artikel Nummer : 110H-MDCARRIER
Lieferant: DOMNICK HUNTER

New Product


Beschreibung: 4000-Stunden-Wartungsset für LCMS 15-0, 2-0, 30-0, 40-0
Artikel-Nr: 564-0006
UOM: 1 * 1 ST
Hersteller Artikel Nummer : 606272253
Lieferant: DOMNICK HUNTER


Beschreibung: This sulpho-SHPP (water-soluble Bolton-Hunter Reagent) is designed to aid the labelling of proteins with radioactive iodine. Radioactive iodine (¹²⁵I) is routinely used by researchers to label proteins. The iodination of proteins can be performed enzymatically or chemically.
Artikel-Nr: BC92
UOM: 1 * 100 mg
Hersteller Artikel Nummer : BC92
Lieferant: G-Biosciences


Beschreibung: Bolton-Hunter reagent (sulpho-SHPP), technische Qualität
Artikel-Nr: APOSBII110-1G
UOM: 1 * 1 g
Hersteller Artikel Nummer : BII110-1G
Lieferant: Apollo Scientific


Beschreibung: Bolton-Hunter reagent (sulpho-SHPP)
Artikel-Nr: APOSBII101-10G
UOM: 1 * 10 g
Hersteller Artikel Nummer : BII101-10G
Lieferant: Apollo Scientific


Beschreibung: Bolton-Hunter reagent (sulpho-SHPP)
Artikel-Nr: J64508.03
UOM: 1 * 1 g
Hersteller Artikel Nummer : J64508.03
Lieferant: Thermo Fisher Scientific

Beschreibung: Defects in GDF5 are the cause of acromesomelic chondrodysplasia Grebe type (AMDG) . Acromesomelic chondrodysplasias are rare hereditary skeletal disorders characterized by short stature, very short limbs, and hand/foot malformations. The severity of limb abnormalities increases from proximal to distal with profoundly affected hands and feet showing brachydactyly and/or rudimentary fingers (knob-like fingers). AMDG is an autosomal recessive form characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of acromesomelic chondrodysplasia Hunter-Thompson type (AMDH). AMDH is an autosomal recessive form of dwarfism. Patients have limb abnormalities, with the middle and distal segments being most affected and the lower limbs more affected than the upper. AMDH is characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of brachydactyly type C (BDC). BDC is an autosomal dominant disorder characterized by an abnormal shortness of the fingers and toes.
Artikel-Nr: BOSSBS-6580R-HRP
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-6580R-HRP
Lieferant: Bioss


Beschreibung: Sulpho-SHPP, sulphosuccinimidyl-3 -(4-hydroxypheynyl) propionate, also known as water-soluble Bolton-Hunter reagent, conjugates tyrosine-like functional groups to primary amines to increase the number of tyrosyl groups that can be iodinated by iodine-125 labeling procedures.
Artikel-Nr: PIER27712
UOM: 1 * 100 mg
Hersteller Artikel Nummer : 27712
Lieferant: Thermo Fisher Scientific


Beschreibung: Defects in GDF5 are the cause of acromesomelic chondrodysplasia Grebe type (AMDG) . Acromesomelic chondrodysplasias are rare hereditary skeletal disorders characterized by short stature, very short limbs, and hand/foot malformations. The severity of limb abnormalities increases from proximal to distal with profoundly affected hands and feet showing brachydactyly and/or rudimentary fingers (knob-like fingers). AMDG is an autosomal recessive form characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of acromesomelic chondrodysplasia Hunter-Thompson type (AMDH). AMDH is an autosomal recessive form of dwarfism. Patients have limb abnormalities, with the middle and distal segments being most affected and the lower limbs more affected than the upper. AMDH is characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of brachydactyly type C (BDC). BDC is an autosomal dominant disorder characterized by an abnormal shortness of the fingers and toes.
Artikel-Nr: BOSSBS-6580R
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-6580R
Lieferant: Bioss


Beschreibung: The protein encoded by this gene is a member of the bone morphogenetic protein (BMP) family and the TGF-beta superfamily. This group of proteins is characterized by a polybasic proteolytic processing site which is cleaved to produce a mature protein containing seven conserved cysteine residues. The members of this family are regulators of cell growth and differentiation in both embryonic and adult tissues. Mutations in this gene are associated with acromesomelic dysplasia, Hunter-Thompson type; brachydactyly, type C; and chondrodysplasia, Grebe type. These associations confirm that the gene product plays a role in skeletal development.
Artikel-Nr: PRSI56-193
UOM: 1 * 400 µl
Hersteller Artikel Nummer : 56-193
Lieferant: ProSci Inc.

New Product


Beschreibung: Eine Serie von Spektralphotometern zur Farbabstufung optisch transparenter Proben. Jede Ausführung des PFX<i>i </i>195 enthält eine Auswahl an in spezifischen Industrien verwendeten Standard-Farbskalen. Weitere Farbskalen können ergänzt werden, bereits bei der Bestellung oder als Nachbestellung zur optionale Erweiterung, um bei individuellen Voraussetzungen flexibel sein zu können. Ergebnisse können auch in Form von Spektraldaten und CIE-Werten dargestellt werden. Für Produkte, die nicht mit der Standardfarbskala des PFX<i>i </i>195 kompartibel sind kann der Anwender eine benutzerdefinierte Skala aus einer Reihe von Referenzproben aufbauen und so die beste Übereinstimmung mit der gespeicherten Referenz zu erhalten.
Artikel-Nr: 633-0221
UOM: 1 * 1 ST
Hersteller Artikel Nummer : 1371959
Lieferant: Lovibond Tintometer


Beschreibung: It is well known that the control of gene expression involves activation of protein kinase cascades that regulate transcription factors within the nucleus (Karin and Hunter, 1995). The cyclic AMP response element binding protein (CREB) is one of the best characterized stimulus-induced transcription factors (Montminy, 1997). This transcription factor is a component of intracellular signaling events that regulate a wide range of biological functions, from spermatogenesis to circadian rhythms and memory (Shaywitz and Greenberg, 1999; Silva et al., 1998). A variety of protein kinases including protein kinase A (PKA), mitogenactivated protein kinases (MAPKs), and Ca2+/calmodulin-dependent protein kinases (CaMKs) phosphorylate CREB at serine 133 (Ser133), and phosphorylation of Ser133 are required for CREB-mediated transcription (Johannessen et al., 2004; Kornhauser et al., 2002).
Artikel-Nr: PRSI50-221
UOM: 1 * 100 µl
Hersteller Artikel Nummer : 50-221
Lieferant: ProSci Inc.


Beschreibung: GEHÖRSCHUTZ PELTOR PROTAC HUNTER GRUN 1 * 1 ST
Artikel-Nr: MMMAMT13H222A
UOM: 1 * 1 ST
Hersteller Artikel Nummer : MT13H222A
Lieferant: 3M


Beschreibung: [EN]AIR ELEMENT 504431110 COMP 1 * 1 ST
Artikel-Nr: DHUN010AA
UOM: 1 * 1 ST
Hersteller Artikel Nummer : 010AA
Lieferant: DOMNICK HUNTER


Beschreibung: INSTALLATION 1 * 1 ST
Artikel-Nr: DHUNINSTALL
UOM: 1 * 1 ST
Hersteller Artikel Nummer : INSTALL
Lieferant: DOMNICK HUNTER


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