Procurou por: VARLP041222ACRO00002

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.

Código de Artigo: BC92

UOM: 1 * 100 mg

Fornecedor: G-Biosciences

Promoção

Descrição: Bolton-Hunter reagent (sulpho-SHPP)

Código de Artigo: APOSBII101-10G

UOM: 1 * 10 g

Fornecedor: Apollo Scientific

Promoção

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

Código de Artigo: APOSBII110-5G

UOM: 1 * 5 g

Fornecedor: Apollo Scientific

Promoção

Descrição: Bolton-Hunter reagent (sulpho-SHPP)

Código de Artigo: J64508.03

UOM: 1 * 1 g

Fornecedor: Thermo Fisher Scientific

MSDS Certificados Promoção

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.

Código de Artigo: PIER27712

UOM: 1 * 100 mg

Fornecedor: Thermo Fisher Scientific

Promoção

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.

Código de Artigo: DHUN110H-MDCARRIER

UOM: 1 * 1 unid.

Fornecedor: DOMNICK HUNTER

Novo produto Promoção

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

Código de Artigo: MFLX29587-11

UOM: 1 * 1 unid.

Fornecedor: Avantor Fluid Handling

Promoção

Descrição: Splinter forceps with lancet tips.

Código de Artigo: 232-0063

UOM: 1 * 1 unid.

Fornecedor: HAMMACHER KARL

Promoção

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.

Código de Artigo: 633-0221

UOM: 1 * 1 unid.

Fornecedor: Lovibond Tintometer

Promoção

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

Código de Artigo: MMMAMT13H222A

UOM: 1 * 1 unid.

Fornecedor: 3M

Promoção

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.

Código de Artigo: PRSI56-193

UOM: 1 * 400 µl

Fornecedor: ProSci Inc.

Promoção

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.

Código de Artigo: BOSSBS-6580R

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

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.

Código de Artigo: BOSSBS-6580R-HRP

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

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).

Código de Artigo: PRSI50-221

UOM: 1 * 100 µl

Fornecedor: ProSci Inc.

Promoção

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

Código de Artigo: 564-0006

UOM: 1 * 1 unid.

Fornecedor: DOMNICK HUNTER

Promoção

Descrição: BOLTON-HUNTER REAGENT 1 * 25 g

Código de Artigo: J64508.14

UOM: 1 * 25 g

Fornecedor: Thermo Fisher Scientific

MSDS Certificados Promoção