Wyszukano: Adenosine

Numer katalogowy: (BOSSBS-7060R-A680)

Producent: Bioss

Opis: NT5C1A dephosphorylates the 5' and 2'(3')-phosphates of deoxyribonucleotides and has a broad substrate specificity. It helps to regulate adenosine levels in the heart during ischemia and hypoxia.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-7060R-HRP)

Producent: Bioss

Opis: NT5C1A dephosphorylates the 5' and 2'(3')-phosphates of deoxyribonucleotides and has a broad substrate specificity. It helps to regulate adenosine levels in the heart during ischemia and hypoxia.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-7060R-FITC)

Producent: Bioss

Opis: NT5C1A dephosphorylates the 5' and 2'(3')-phosphates of deoxyribonucleotides and has a broad substrate specificity. It helps to regulate adenosine levels in the heart during ischemia and hypoxia.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-6248R-A750)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-6248R-A647)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-6248R-A350)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-7060R-A750)

Producent: Bioss

Opis: NT5C1A dephosphorylates the 5' and 2'(3')-phosphates of deoxyribonucleotides and has a broad substrate specificity. It helps to regulate adenosine levels in the heart during ischemia and hypoxia.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-7060R-A488)

Producent: Bioss

Opis: NT5C1A dephosphorylates the 5' and 2'(3')-phosphates of deoxyribonucleotides and has a broad substrate specificity. It helps to regulate adenosine levels in the heart during ischemia and hypoxia.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-7060R-A647)

Producent: Bioss

Opis: NT5C1A dephosphorylates the 5' and 2'(3')-phosphates of deoxyribonucleotides and has a broad substrate specificity. It helps to regulate adenosine levels in the heart during ischemia and hypoxia.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-12529R-FITC)

Producent: Bioss

Opis: Actin-related proteins are classified into Arp subclasses according to their amino acid sequence similarity to Actin. Both Arps and Actin proteins have an ATPase domain, which catalyzes the decomposition of adenosine triphosphate (ATP) into adenosine diphosphate (ADP) and a free phosphate ion to release energy. ArpM1 (actin-related protein M1) is a 372 amino acid ubiquitously expressed protein that localizes to both the cytoplasm and the cytoskeleton and belongs to the Arp family of Actin-like proteins. The gene encoding ArpM1 maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-12529R-CY7)

Producent: Bioss

Opis: Actin-related proteins are classified into Arp subclasses according to their amino acid sequence similarity to Actin. Both Arps and Actin proteins have an ATPase domain, which catalyzes the decomposition of adenosine triphosphate (ATP) into adenosine diphosphate (ADP) and a free phosphate ion to release energy. ArpM1 (actin-related protein M1) is a 372 amino acid ubiquitously expressed protein that localizes to both the cytoplasm and the cytoskeleton and belongs to the Arp family of Actin-like proteins. The gene encoding ArpM1 maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-12529R-A750)

Producent: Bioss

Opis: Actin-related proteins are classified into Arp subclasses according to their amino acid sequence similarity to Actin. Both Arps and Actin proteins have an ATPase domain, which catalyses the decomposition of adenosine triphosphate (ATP) into adenosine diphosphate (ADP) and a free phosphate ion to release energy. ArpM1 (actin-related protein M1) is a 372 amino acid ubiquitously expressed protein that localizes to both the cytoplasm and the cytoskeleton and belongs to the Arp family of Actin-like proteins. The gene encoding ArpM1 maps to human chromosome 3, which houses over 1100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-12529R-HRP)

Producent: Bioss

Opis: Actin-related proteins are classified into Arp subclasses according to their amino acid sequence similarity to Actin. Both Arps and Actin proteins have an ATPase domain, which catalyzes the decomposition of adenosine triphosphate (ATP) into adenosine diphosphate (ADP) and a free phosphate ion to release energy. ArpM1 (actin-related protein M1) is a 372 amino acid ubiquitously expressed protein that localizes to both the cytoplasm and the cytoskeleton and belongs to the Arp family of Actin-like proteins. The gene encoding ArpM1 maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-12529R-CY5)

Producent: Bioss

Opis: Actin-related proteins are classified into Arp subclasses according to their amino acid sequence similarity to Actin. Both Arps and Actin proteins have an ATPase domain, which catalyzes the decomposition of adenosine triphosphate (ATP) into adenosine diphosphate (ADP) and a free phosphate ion to release energy. ArpM1 (actin-related protein M1) is a 372 amino acid ubiquitously expressed protein that localizes to both the cytoplasm and the cytoskeleton and belongs to the Arp family of Actin-like proteins. The gene encoding ArpM1 maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-12529R-A680)

Producent: Bioss

Opis: Actin-related proteins are classified into Arp subclasses according to their amino acid sequence similarity to Actin. Both Arps and Actin proteins have an ATPase domain, which catalyses the decomposition of adenosine triphosphate (ATP) into adenosine diphosphate (ADP) and a free phosphate ion to release energy. ArpM1 (actin-related protein M1) is a 372 amino acid ubiquitously expressed protein that localizes to both the cytoplasm and the cytoskeleton and belongs to the Arp family of Actin-like proteins. The gene encoding ArpM1 maps to human chromosome 3, which houses over 1100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-6248R-A488)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

Wyprzedaż