Human ALPL protein (Recombinant) (N-His) (STJP003717)

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STJP003717
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Host: E. coli
Note: STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Short Description : Recombinant-Human ALPL-N-His protein was developed from e. coli and has a target region of N-His. For use in research applications.
Formulation: Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Storage Instruction: Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at-20 to-80°C for twelve months from the date of receipt.
Gene Symbol: ALPL
Gene ID: 249
Uniprot ID: PPBT_HUMAN
Immunogen Region: Leu18-Ser501
Immunogen: Homo sapiens (Human)
Function Alkaline phosphatase that metabolizes various phosphate compounds and plays a key role in skeletal mineralization and adaptive thermogenesis. Has broad substrate specificity and can hydrolyze a considerable variety of compounds: however, only a few substrates, such as diphosphate (inorganic pyrophosphate.PPi), pyridoxal 5'-phosphate (PLP) and N-phosphocreatine are natural substrates. Plays an essential role in skeletal and dental mineralization via its ability to hydrolyze extracellular diphosphate, a potent mineralization inhibitor, to phosphate: it thereby promotes hydroxyapatite crystal formation and increases inorganic phosphate concentration. Acts in a non-redundant manner with PHOSPHO1 in skeletal mineralization: while PHOSPHO1 mediates the initiation of hydroxyapatite crystallization in the matrix vesicles (MVs), ALPL/TNAP catalyzes the spread of hydroxyapatite crystallization in the extracellular matrix. Also promotes dephosphorylation of osteopontin (SSP1), an inhibitor of hydroxyapatite crystallization in its phosphorylated state.it is however unclear whether ALPL/TNAP mediates SSP1 dephosphorylation via a direct or indirect manner. Catalyzes dephosphorylation of PLP to pyridoxal (PL), the transportable form of vitamin B6, in order to provide a sufficient amount of PLP in the brain, an essential cofactor for enzymes catalyzing the synthesis of diverse neurotransmitters. Additionally, also able to mediate ATP degradation in a stepwise manner to adenosine, thereby regulating the availability of ligands for purinergic receptors. Also capable of dephosphorylating microbial products, such as lipopolysaccharides (LPS) as well as other phosphorylated small-molecules, such as poly-inosine:cytosine (poly I:C). Acts as a key regulator of adaptive thermogenesis as part of the futile creatine cycle: localizes to the mitochondria of thermogenic fat cells and acts by mediating hydrolysis of N-phosphocreatine to initiate a futile cycle of creatine dephosphorylation and phosphorylation. During the futile creatine cycle, creatine and N-phosphocreatine are in a futile cycle, which dissipates the high energy charge of N-phosphocreatine as heat without performing any mechanical or chemical work.
Protein Name Alkaline Phosphatase - Tissue-Nonspecific Isozyme
Ap-Tnap
Tns-Alp
Tnsalp
Alkaline Phosphatase Liver/Bone/Kidney Isozyme
Phosphoamidase
Phosphocreatine Phosphatase
Database Links Reactome: R-HSA-163125
Cellular Localisation Cell Membrane
Lipid-Anchor
Gpi-Anchor
Extracellular Vesicle Membrane
Mitochondrion Membrane
Mitochondrion Intermembrane Space
Localizes To Special Class Of Extracellular Vesicles
Named Matrix Vesicles (Mvs)
Which Are Released By Osteogenic Cells
Localizes To The Mitochondria Of Thermogenic Fat Cells: Tethered To Mitochondrial Membranes Via A Gpi-Anchor And Probably Resides In The Mitochondrion Intermembrane Space
Alternative Protein Names Alkaline Phosphatase - Tissue-Nonspecific Isozyme protein
Ap-Tnap protein
Tns-Alp protein
Tnsalp protein
Alkaline Phosphatase Liver/Bone/Kidney Isozyme protein
Phosphoamidase protein
Phosphocreatine Phosphatase protein
ALPL protein

Information sourced from Uniprot.org