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Human PKLR ELISA Kit für Sandwich ELISA - ABIN414647
Ren, Yang, Wang, Ma: The effects of PGC-1α on the proliferation and energy metabolism of malignant endometrial cancer cells. in OncoTargets and therapy 2015
Show all 2 Pubmed References
AMPD3 deficiency increases the level of ATP in erythrocytes, but does not improve anemia due to pyruvate kinase deficiency and leads to erythrocyte dysfunction.
Pyruvate kinase deficiency in mice protects against malaria
Gene copy number variation (CNV) of the PKLR, FCGR2A (zeige FCGR2A ELISA Kits), FCGR2C, and FCGR3 (zeige CD16 ELISA Kits) genes is associated with malaria severity, and our results provide evidence for a role of CNV in host responses to malaria.
Genotype-phenotype correlations for the novel missense mutations found in the PKLR gene in PK deficiency among Tunisian cases were investigated by three-dimensional structure analysis.
Data show that pyruvate kinase (PK) activity was decreased in the GATA1 (zeige GATA1 ELISA Kits) hemizygous state and PKLR c.1284delA variant.
An update of PKLR gene mutation database has been presented. (Review)
Two Novel Missense Mutations and a 5bp Deletion in the Erythroid-Specific Promoter of the PKLR Gene in Two Unrelated Patients With Pyruvate Kinase Deficient Transfusion-Dependent Chronic Nonspherocytic Hemolytic Anemia.
PKLR promotes colorectal cancer liver colonization through induction of glutathione synthesis.
Pyruvate kinase variants modulate malaria phenotypes in a Thai population.
661G>A and 1528C>T mutations of PKLR gene are associated with pyruvate kinase deficiency.
Case Report: unknown mutation in the pyruvate kinase gene (PKLR) identified from a neonate with severe jaundice.
This study determined which interactions in the fructose 1,6-bisphosphate binding site of human liver pyruvate kinase contribute to allostery.
The existence of mitochondrial Pyruvate kinase was confirmed by immunological analysis in pig liver mitochondria.
The protein encoded by this gene is a pyruvate kinase that catalyzes the transphosphorylation of phohsphoenolpyruvate into pyruvate and ATP, which is the rate-limiting step of glycolysis. Defects in this enzyme, due to gene mutations or genetic variations, are the common cause of chronic hereditary nonspherocytic hemolytic anemia (CNSHA or HNSHA). Multiple transcript variants encoding different isoforms have been found for this gene.
pyruvate kinase isozymes R/L
, pyruvate kinase, liver and RBC
, Pyruvate kinase isozyme R
, pyruvate kinase isozymes R/L-like
, pyruvate kinase PKLR
, pyruvate kinase isozymes L/R
, R-type/L-type pyruvate kinase
, pyruvate kinase 1
, pyruvate kinase isozyme R/L
, pyruvate kinase type L
, pyruvate kinase, liver and blood cell
, red cell/liver pyruvate kinase
, Pyruvate kinase isozymes R/L
, pyruvate kinase, liver and red blood cell