Sie suchten nach: DOMNICK+HUNTER

Lieferant: Avantor Fluid Handling

Beschreibung: Advanced airflow technology makes this the most energy efficient compressed air filtration system available.

Lieferant: DOMNICK HUNTER GMBH

Beschreibung: 4000-Stunden-Wartungsset für LCMS 15-0, 2-0, 30-0, 40-0

Artikel-Nr: (DHUN110H-MDCARRIER)

Lieferant: DOMNICK HUNTER

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.

VE: 1 * 1 ST

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Artikel-Nr: (BC92)

Lieferant: G-Biosciences

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.

VE: 1 * 100 mg

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Lieferant: Apollo Scientific

Beschreibung: Bolton-Hunter reagent (sulpho-SHPP), technische Qualität

Lieferant: Apollo Scientific

Beschreibung: Bolton-Hunter reagent (sulpho-SHPP)

Artikel-Nr: (J64508.03)

Lieferant: Thermo Scientific

Beschreibung: Bolton-Hunter reagent (sulpho-SHPP)

VE: 1 * 1 g

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Artikel-Nr: (BOSSBS-6580R-HRP)

Lieferant: Bioss

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.

VE: 1 * 100 µl

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Artikel-Nr: (BOSSBS-6580R)

Lieferant: Bioss

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.

VE: 1 * 100 µl

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Artikel-Nr: (PIER27712)

Lieferant: Thermo Fisher Scientific

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.

VE: 1 * 100 mg

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Artikel-Nr: (232-0063)

Lieferant: HAMMACHER KARL

Beschreibung: Splinter forceps with lancet tips.

VE: 1 * 1 ST

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Artikel-Nr: (PRSI56-193)

Lieferant: ProSci Inc.

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.

VE: 1 * 400 µl

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Artikel-Nr: (633-0221)

Lieferant: Lovibond Tintometer

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.

VE: 1 * 1 ST

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Artikel-Nr: (STMC78083.1)

Lieferant: STEMCELL Technologies

Beschreibung: Interleukin 6 receptor (IL-6R) alpha is a type I transmembrane glycoprotein that forms a complex with type I transmembrane signal transducer protein gp130 (CD130) and mediates the biological activities of IL-6. IL-6 binds to the membrane-bound non-signaling IL-6R alpha (mIL-6R), and the complex binds to two molecules of gp130 and leads to ‘classical’ IL-6-signal transduction, which includes activation of JAK/STAT, ERK, and PI3K signal transduction pathways (Scheller <i>et al.</i>). In contrast, a soluble form of IL-6R alpha (sIL-6R), which comprises the extracellular portion of the receptor, binds to the secreted IL-6 to form a complex that promotes bioavailability of IL-6. The complex of IL-6 and sIL-6R can bind to gp130 on cells that do not express the IL-6R and are unresponsive to IL-6. This process is known as trans-signaling (Hunter and Jones; Rose-John S). sIL-6R regulates both local and systemic IL-6-mediated events. Elevated levels of sIL-6R have been documented in several disease conditions such as rheumatoid arthritis, myeloma, and Crohn’s disease (Jones <i>et al.</i>; Mihara <i>et al.</i>).

VE: 1 * 50 µG

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Artikel-Nr: (PRSI50-221)

Lieferant: ProSci Inc.

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).

VE: 1 * 100 µl

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Artikel-Nr: (MMMAMT13H222A)

Lieferant: 3M

Beschreibung: GEHRSCHUTZ PELTOR PROTAC HUNTER GRUN 1 * 1 ST

VE: 1 * 1 ST

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