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SDS-PAGE

Alkaline phosphatase, tissue-nonspecific isozyme Recombinant Protein | Alpl recombinant protein

Recombinant Mouse Alkaline phosphatase, tissue-nonspecific isozyme

Gene Names
Alpl; Akp2; TNAP; Akp-2; APTNAP; TNSALP
Purity
Greater or equal to 85% purity as determined by SDS-PAGE.
Synonyms
Alkaline phosphatase; tissue-nonspecific isozyme; Recombinant Mouse Alkaline phosphatase; Alkaline phosphatase 2; Alkaline phosphatase liver/bone/kidney isozyme; Alpl recombinant protein
Ordering
For Research Use Only!
Host
E Coli
Purity/Purification
Greater or equal to 85% purity as determined by SDS-PAGE.
Form/Format
Liquid containing glycerol
Sequence Positions
20-503aa; Partial
Sequence
PEKERDPSYWRQQAQETLKNALKLQKLNTNVAKNVIMFLGDGMGVSTVTAARILKGQLHHNTGEETRLEMDKFPFVALSKTYNTNAQVPDSAGTATAYLCGVKANEGTVGVSAATERTRCNTTQGNEVTSILRWAKDAGKSVGIVTTTRVNHATPSAAYAHSADRDWYSDNEMPPEALSQGCKDIAYQLMHNIKDIDVIMGGGRKYMYPKNRTDVEYELDEKARGTRLDGLDLISIWKSFKPRHKHSHYVWNRTELLALDPSRVDYLLGLFEPGDMQYELNRNNLTDPSLSEMVEVALRILTKNLKGFFLLVEGGRIDHGHHEGKAKQALHEAVEMDQAIGKAGAMTSQKDTLTVVTADHSHVFTFGGYTPRGNSIFGLAPMVSDTDKKPFTAILYGNGPGYKVVDGERENVSMVDYAHNNYQAQSAVPLRHETHGGEDVAVFAKGPMAHLLHGVHEQNYIPHVMAYASCIGANLDHCAWAGSG
Sequence Length
503
Preparation and Storage
Store at -20 degree C, for extended storage, conserve at -20 degree C or -80 degree C.

SDS-PAGE

SDS-PAGE
References
Cloning and characterization of a cDNA coding for mouse placental alkaline phosphatase.Terao M., Mintz B.Proc. Natl. Acad. Sci. U.S.A. 84:7051-7055(1987) Lineage-specific biology revealed by a finished genome assembly of the mouse.Church D.M., Goodstadt L., Hillier L.W., Zody M.C., Goldstein S., She X., Bult C.J., Agarwala R., Cherry J.L., DiCuccio M., Hlavina W., Kapustin Y., Meric P., Maglott D., Birtle Z., Marques A.C., Graves T., Zhou S., Teague B., Potamousis K., Churas C., Place M., Herschleb J., Runnheim R., Forrest D., Amos-Landgraf J., Schwartz D.C., Cheng Z., Lindblad-Toh K., Eichler E.E., Ponting C.P.PLoS Biol. 7:E1000112-E1000112(2009) Induction of alkaline phosphatase in mouse L cells by overexpression of the catalytic subunit of cAMP-dependent protein kinase.Brown N.A., Stofko R.E., Uhler M.D.J. Biol. Chem. 265:13181-13189(1990) Mass-spectrometric identification and relative quantification of N-linked cell surface glycoproteins.Wollscheid B., Bausch-Fluck D., Henderson C., O'Brien R., Bibel M., Schiess R., Aebersold R., Watts J.D.Nat. Biotechnol. 27:378-386(2009)

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
57.4 kDa
NCBI Official Full Name
alkaline phosphatase, tissue-nonspecific isozyme preproprotein
NCBI Official Synonym Full Names
alkaline phosphatase, liver/bone/kidney
NCBI Official Symbol
Alpl
NCBI Official Synonym Symbols
Akp2; TNAP; Akp-2; APTNAP; TNSALP
NCBI Protein Information
alkaline phosphatase, tissue-nonspecific isozyme
UniProt Protein Name
Alkaline phosphatase, tissue-nonspecific isozyme
Protein Family
UniProt Gene Name
Alpl
UniProt Synonym Gene Names
Akp-2; Akp2; AP-TNAP; TNSALP
UniProt Entry Name
PPBT_MOUSE

NCBI Description

This gene encodes a preproprotein that is proteolytically cleaved to yield a signal peptide and a proproptein that is subsequently processed to generate the active mature peptide. The encoded protein is a membrane-bound glycosylated enzyme that catalyzes the hydrolysis of phosphate esters at alkaline pH. The mature peptide maintains the ratio of inorganic phosphate to inorganic pyrophosphate required for bone mineralization. Mice that lack this enzyme show symptoms of osteomalacia, softening of the bones. In humans, mutations in this gene are associated with hypophosphatasia, an inherited metabolic bone disease in which deficiency of this enzyme inhibits bone mineralization leading to skeletal defects. Mutations in the mouse gene mirror the symptoms of human hypophosphatasia. A pseudogene of this gene is present on chromosome X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]

Uniprot Description

ALPL: This isozyme may play a role in skeletal mineralization. Defects in ALPL are a cause of hypophosphatasia (HOPS). HOPS is an inherited metabolic bone disease characterized by defective skeletal mineralization. Four hypophosphatasia forms are distinguished, depending on the age of onset: perinatal, infantile, childhood and adult type. The perinatal form is the most severe and is almost always fatal. Patients with only premature loss of deciduous teeth, but with no bone disease are regarded as having odontohypophosphatasia (odonto). Defects in ALPL are a cause of hypophosphatasia childhood type (HOPSC). Defects in ALPL are a cause of hypophosphatasia infantile type (HOPSI). Belongs to the alkaline phosphatase family. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Cofactor and Vitamin Metabolism - folate biosynthesis; EC 3.1.3.1; Membrane protein, GPI anchor; Phosphatase (non-protein); Motility/polarity/chemotaxis

Cellular Component: extracellular space; membrane; plasma membrane; proteinaceous extracellular matrix

Molecular Function: alkaline phosphatase activity; catalytic activity; hydrolase activity; metal ion binding; phosphoric monoester hydrolase activity; protein binding; pyrophosphatase activity

Biological Process: dephosphorylation; endochondral ossification; metabolic process; osteoblast differentiation; reproductive developmental process; response to antibiotic; response to glucocorticoid stimulus

Research Articles on Alpl

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Product Notes

The Alpl alpl (Catalog #AAA1265539) is a Recombinant Protein produced from E Coli and is intended for research purposes only. The product is available for immediate purchase. The immunogen sequence is 20-503aa; Partial. The amino acid sequence is listed below: PEKERDPSYW RQQAQETLKN ALKLQKLNTN VAKNVIMFLG DGMGVSTVTA ARILKGQLHH NTGEETRLEM DKFPFVALSK TYNTNAQVPD SAGTATAYLC GVKANEGTVG VSAATERTRC NTTQGNEVTS ILRWAKDAGK SVGIVTTTRV NHATPSAAYA HSADRDWYSD NEMPPEALSQ GCKDIAYQLM HNIKDIDVIM GGGRKYMYPK NRTDVEYELD EKARGTRLDG LDLISIWKSF KPRHKHSHYV WNRTELLALD PSRVDYLLGL FEPGDMQYEL NRNNLTDPSL SEMVEVALRI LTKNLKGFFL LVEGGRIDHG HHEGKAKQAL HEAVEMDQAI GKAGAMTSQK DTLTVVTADH SHVFTFGGYT PRGNSIFGLA PMVSDTDKKP FTAILYGNGP GYKVVDGERE NVSMVDYAHN NYQAQSAVPL RHETHGGEDV AVFAKGPMAH LLHGVHEQNY IPHVMAYASC IGANLDHCAW AGSG. It is sometimes possible for the material contained within the vial of "Alkaline phosphatase, tissue-nonspecific isozyme, Recombinant Protein" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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