Procurou por: DOMNICK+HUNTER

Fornecedor: Avantor Fluid Handling

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

Código de Artigo: (DHUN110H-MDCARRIER)

Fornecedor: DOMNICK HUNTER

Descrição: Os geradores de hidrogénio Parker Domnick Hunter produzem um fluxo contínuo de hidrogénio puro a partir de água desionizada. Estes geradores de hidrogénio constituem uma alternativa segura e simples aos cilindros de gás de alta pressão. O hidrogénio só é produzido a baixa pressão quando solicitado e o volume de gás armazenado é mínimo.

UOM: 1 * 1 unid.

Novo produto Promoção

Fornecedor: DOMNICK HUNTER

Descrição: Kit de manutenção para 4000 horas para todos os LCMS

Código de Artigo: (BC92)

Fornecedor: G-Biosciences

Descrição: 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.

UOM: 1 * 100 mg

Promoção

Fornecedor: Apollo Scientific

Descrição: Bolton-Hunter reagent (sulpho-SHPP), Technical Grade

Fornecedor: Apollo Scientific

Descrição: Bolton-Hunter reagent (sulpho-SHPP)

Código de Artigo: (J64508.03)

Fornecedor: Thermo Fisher Scientific

Descrição: Bolton-Hunter reagent (sulpho-SHPP)

UOM: 1 * 1 g

MSDS Certificados Promoção

Código de Artigo: (PIER27712)

Fornecedor: Thermo Fisher Scientific

Descrição: 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.

UOM: 1 * 100 mg

Promoção

Código de Artigo: (232-0063)

Fornecedor: HAMMACHER KARL

Descrição: Splinter forceps with lancet tips.

UOM: 1 * 1 unid.

Promoção

Código de Artigo: (BOSSBS-6580R-HRP)

Fornecedor: Bioss

Descrição: 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.

UOM: 1 * 100 µl

Promoção

Código de Artigo: (BOSSBS-6580R)

Fornecedor: Bioss

Descrição: 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.

UOM: 1 * 100 µl

Promoção

Código de Artigo: (PRSI56-193)

Fornecedor: ProSci Inc.

Descrição: 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.

UOM: 1 * 400 µl

Promoção

Código de Artigo: (633-0221)

Fornecedor: Lovibond Tintometer

Descrição: Uma série de colorímetros espectrofotométricos para graduação de cor de amostras transparentes. Cada versão do PFX<i>i </i>195 inclui uma selecção de escalas de cores standard utilizada num sector industrial específico. Podem ser acrescentadas mais escalas, no momento da encomenda ou à distância, como actualizações opcionais para assegurar a flexibilidade que permite satisfazer as necessidades individuais. Os resultados também podem ser exibidos em termos de dados espectrais e valores CIE. Para tipos de produtos que são incompatíveis com as escalas de cores standard, o software do PFX<i>i </i>195 permite aos utilizadores a criação de uma escala personalizada a partir de uma série de amostras de referência, para que se obtenha posteriormente a alternativa mais aproximada à referência armazenada.

UOM: 1 * 1 unid.

Promoção

Código de Artigo: (PRSI50-221)

Fornecedor: ProSci Inc.

Descrição: 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).

UOM: 1 * 100 µl

Promoção

Código de Artigo: (STMC78083.1)

Fornecedor: STEMCELL TECHNOLOGIES

Descrição: 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>).

UOM: 1 * 50 µG

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Código de Artigo: (MMMAMT13H222A)

Fornecedor: 3M

Descrição: [EN]EARMUFF PELTOR PROTAC HUNTER GREEN 1 * 1 unid.

UOM: 1 * 1 unid.

Promoção