Search results for kinase 1

Checkpoint Kinase 1 (CHEK1) Antibody, Abbexa, abx314788

CHEK1 Antibody is a Rabbit Polyclonal against CHEK1.

Adenylate kinase 1 antibody [N1C3], Genetex, GTX106079

Pantothenate Kinase 1 (PANK1) Antibody, Abbexa, abx301244

PANK1 Antibody is a Rabbit Polyclonal against PANK1.

Phosphoglycerate Kinase 1 (PGK1) Antibody, Abbexa, abx241044

PGK1 Antibody is a Rabbit Polyclonal against PGK1.

Rio Kinase 1 (Yeast) Antibody, Abbexa, abx115304

Rio Kinase 1 (Yeast) Antibody is a Rabbit Polyclonal antibody against Rio Kinase 1 (Yeast).

Phosphoglycerate kinase 1 Antibody (HRP), Abbexa, abx108610

Phosphoglycerate kinase 1 Antibody (HRP) is a Rabbit Polyclonal antibody against Phosphoglycerate kinase 1 conjugated to HRP.

Adenylate Kinase 1 (AK1) Antibody, Abbexa, abx013355

Rabbit polyclonal antibody against KAD1 protein. Immunogen region is Internal.

Phosphoglycerate Kinase 1 (PGK1) Antibody, Abbexa, abx001601

PGK1 Antibody is a Rabbit Polyclonal antibody against PGK1. The PGK1 gene encodes phosphoglycerate kinase-1, also known as ATP:3-phosphoglycerate 1-phosphotransferase (EC 2.7.2.3), which catalyzes the reversible conversion of 1,3-diphosphoglycerate to 3-phosphoglycerate during glycolysis, generating one molecule of ATP. It Belongs to the phosphoglycerate kinase family and defects in PGK1 are the cause of phosphoglycerate kinase 1 deficiency (PGK1D).

Checkpoint Kinase 1 (CHEK1) Antibody, Abbexa, abx324715

CHEK1 Antibody is a Rabbit Polyclonal against CHEK1.

Adenylate Kinase 1 (AK1) Antibody, Abbexa, abx001130

AK1 Antibody is a Rabbit Polyclonal antibody against AK1. Adenylate kinase is an enzyme involved in regulating the adenine nucleotide composition within a cell by catalyzing the reversible transfer of phosphate group among adinine nucleotides. Three isozymes of adenylate kinase have been identified in vertebrates, adenylate isozyme 1 (AK1), 2 (AK2) and 3 (AK3). AK1 is found in the cytosol of skeletal muscle, brain and erythrocytes, whereas AK2 and AK3 are found in the mitochondria of other tissues including liver and heart. AK1 was identified because of its association with a rare genetic disorder causing nonspherocytic hemolytic anemia where a mutation in the AK1 gene was found to reduce the catalytic activity of the enzyme. [provided by RefSeq, Jul 2008].