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Human Polyclonal PFKL Primary Antibody for IHC (p), ELISA - ABIN544923
Elson, Levanon, Brandeis, Dafni, Bernstein, Danciger, Groner: The structure of the human liver-type phosphofructokinase gene. in Genomics 1990
Show all 3 Pubmed References
Human Polyclonal PFKL Primary Antibody for IHC (p), WB - ABIN392745
Mikawa, Maruyama, Okamoto, Nakagama, Lleonart, Tsusaka, Hori, Murakami, Izumi, Takaori-Kondo, Yokode, Peters, Beach, Kondoh: Senescence-inducing stress promotes proteolysis of phosphoglycerate mutase via ubiquitin ligase Mdm2. in The Journal of cell biology 2014
Cow (Bovine) Polyclonal PFKL Primary Antibody for WB - ABIN2782359
Spellman, Ahmed, Dubach, Gardiner: Expression of trisomic proteins in Down syndrome model systems. in Gene 2012
Human Polyclonal PFKL Primary Antibody for WB - ABIN6243832
Rueda, Johnson, Giddabasappa, Swaroop, Brooks, Sigel, Chaney, Fox: The cellular and compartmental profile of mouse retinal glycolysis, tricarboxylic acid cycle, oxidative phosphorylation, and ~P transferring kinases. in Molecular vision 2016
Liver PFK1 isoform assembles into filaments in a tetramer- and substrate-dependent manner,organizing isoform specific glucose metabolism in cells.
findings showed glycosylation inhibited PFK1 activity and redirected glucose flux through the pentose phosphate pathway, thereby conferring a selective growth advantage on cancer cells
insulin, the most known regulator of glucose consumption, specifically regulates the expression of PFKL and PFKM, which impact the regulation of glycolysis in the cell.
Phosphofructokinase (PFK) is a tetrameric enzyme that catalyzes a key step in glycolysis, namely the conversion of D-fructose 6-phosphate to D-fructose 1,6-bisphosphate. Separate genes encode a muscle subunit (M) and a liver subunit (L). PFK from muscle is a homotetramer of M subunits, PFK from liver is a homotetramer of L-subunits, while PFK from platelets can be composed of any tetrameric combination of M and L subunits. The protein encoded by this gene represents the L subunit. Alternate splicing results in two transcript variants, one of which is a candidate for nonsense-mediated decay (NMD).
6-phosphofructokinase, liver type
, liver-type 1-phosphofructokinase
, phosphofructo-1-kinase isozyme B
, phosphofructokinase 1
, phosphofructokinase, liver, B-type
, phosphofructokinase, liver type