Procurou por: Dibutylboron+trifluoromethanesulphonate

Descrição: Three-prime-phosphoadenosine 5-prime-phosphosulfate (PAPS) is the sulfate donor cosubstrate for all sulfotransferase (SULT) enzymes (Xu et al., 2000 [PubMed 10679223]). SULTs catalyze the sulfate conjugation of many endogenous and exogenous compounds, including drugs and other xenobiotics. In humans, PAPS is synthesized from adenosine 5-prime triphosphate (ATP) and inorganic sulfate by 2 isoforms, PAPSS1 and PAPSS2 (MIM 603005).[supplied by OMIM, Mar 2008].

Código de Artigo: BOSSBS-9029R

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

Descrição: Anti-PAP Mouse Monoclonal Antibody [clone: LT3D1]

Código de Artigo: ABCAAB61707-100

UOM: 1 * 100 µG

Fornecedor: Abcam

Promoção

Descrição: Anti-PAP Rabbit Monoclonal Antibody [clone: SP313]

Código de Artigo: ABCAAB224802-100

UOM: 1 * 100 µl

Fornecedor: Abcam

Promoção

Descrição: The IHC PAP pen provides a hydrophobic barrier when a circle is drawn around a specimen on a glass slide.

Código de Artigo: ENZOADI9502320001

UOM: 1 * 1 unid.

Fornecedor: ENZO LIFE SCIENCES

Promoção

Descrição: Anti-REG3A Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Código de Artigo: USBI040946-FITC

UOM: 1 * 200 µl

Fornecedor: US Biological

Promoção

Descrição: Converts adenosine 3'-phosphate 5'-phosphosulfate (PAPS) to adenosine 5'-phosphosulfate (APS) and 3'(2')-phosphoadenosine 5'- phosphate (PAP) to AMP. Has 1000-fold lower activity towards inositol 1,4-bisphosphate (Ins(1,4)P2) and inositol 1,3,4-trisphosphate (Ins(1,3,4)P3), but does not hydrolyse Ins(1)P, Ins(3,4)P2, Ins(1,3,4,5)P4 or InsP6.

Código de Artigo: BOSSBS-20136R-A750

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

Descrição: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Código de Artigo: BOSSBS-6248R

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

Descrição: Reg protein is stimulated during the regeneration of pancreatic islets. In human, there are four REG family genes; REG 1 alpha, REG 1 beta, REG-related sequence (RS) and HIP/PAP. These Reg-related proteins are classified into four subfamilies according to their amino-acid sequences, but they share a similar structure and physiological function.

Código de Artigo: BOSSBS-6183R-CY7

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

Descrição: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localised to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Código de Artigo: BOSSBS-6248R-A680

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

Descrição: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Código de Artigo: BOSSBS-6248R-CY3

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

Descrição: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Código de Artigo: BOSSBS-6248R-FITC

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

Descrição: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Código de Artigo: BOSSBS-6248R-A555

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

Descrição: Reg protein is stimulated during the regeneration of pancreatic islets. In human, there are four REG family genes; REG 1 alpha, REG 1 beta, REG-related sequence (RS) and HIP/PAP. These Reg-related proteins are classified into four subfamilies according to their amino-acid sequences, but they share a similar structure and physiological function.

Código de Artigo: BOSSBS-6183R-CY5.5

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

Descrição: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Código de Artigo: BOSSBS-6248R-CY7

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

Descrição: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Código de Artigo: BOSSBS-6248R-CY5

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção

Descrição: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Código de Artigo: BOSSBS-6248R-HRP

UOM: 1 * 100 µl

Fornecedor: Bioss

Promoção