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Rat Alkaline Phosphatase (Germ type) /ALPG Protein 2484

$315.00$1,050.00

Summary

  • Expression: HEK293
  • Pure: Yes (HPLC)
  • Amino Acid Range: Val22-Pro510
SKU: 2484parent Categories: , Tag:
Weight1 lbs
Dimensions9 × 5 × 2 in
accession

F1M8U7

express system

HEK293

product tag

C-His

purity

> 95% as determined by Tris-Bis PAGE;> 95% as determined by HPLC

background

Alkaline phosphatase can be considered "our favorite enzyme" for reasons apparent to those who diagnose and treat metabolic bone diseases or who study skeletal biology. Few might know, however, that alkaline phosphatase likely represents the most frequently assayed enzyme in all of medicine. Elevated activity in the circulation is universally recognized as a marker for skeletal or hepatobiliary disease.

molecular weight

The protein has a predicted MW of 54.10 kDa. Due to glycosylation, the protein migrates to 55-70 kDa based on Tris-Bis PAGE result.

available size

100 µg, 500 µg

endotoxin

Less than 1EU per μg by the LAL method.

Rat Alkaline Phosphatase (Germ type) /ALPG Protein 2484

protein
Size and concentration
100, 500µg and lyophilized
Form
Lyophilized
Storage Instructions
Valid for 12 months from date of receipt when stored at -80°C. Recommend to aliquot the protein into smaller quantities for optimal storage. Please minimize freeze-thaw cycles.
Storage buffer
Shipped at ambient temperature.
Purity
> 95% as determined by Tris-Bis PAGE
target relevance
Alkaline phosphatase can be considered "our favorite enzyme" for reasons apparent to those who diagnose and treat metabolic bone diseases or who study skeletal biology. Few might know, however, that alkaline phosphatase likely represents the most frequently assayed enzyme in all of medicine. Elevated activity in the circulation is universally recognized as a marker for skeletal or hepatobiliary disease.
Protein names
Alkaline phosphatase (EC 3.1.3.1)
Gene names
Alpg,Alpg Alppl2
Protein family
Alkaline phosphatase family
Mass
10116Da
Catalytic activity
BINDING 63; /ligand="Mg(2+)"; /ligand_id="ChEBI:CHEBI:18420"; /evidence="ECO:0000256|PIRSR:PIRSR601952-2"; BINDING 63; /ligand="Zn(2+)"; /ligand_id="ChEBI:CHEBI:29105"; /ligand_label="2"; /evidence="ECO:0000256|PIRSR:PIRSR601952-2"; BINDING 174; /ligand="Mg(2+)"; /ligand_id="ChEBI:CHEBI:18420"; /evidence="ECO:0000256|PIRSR:PIRSR601952-2"; BINDING 176; /ligand="Mg(2+)"; /ligand_id="ChEBI:CHEBI:18420"; /evidence="ECO:0000256|PIRSR:PIRSR601952-2"; BINDING 332; /ligand="Mg(2+)"; /ligand_id="ChEBI:CHEBI:18420"; /evidence="ECO:0000256|PIRSR:PIRSR601952-2"; BINDING 337; /ligand="Zn(2+)"; /ligand_id="ChEBI:CHEBI:29105"; /ligand_label="2"; /evidence="ECO:0000256|PIRSR:PIRSR601952-2"; BINDING 341; /ligand="Zn(2+)"; /ligand_id="ChEBI:CHEBI:29105"; /ligand_label="2"; /evidence="ECO:0000256|PIRSR:PIRSR601952-2"; BINDING 378; /ligand="Zn(2+)"; /ligand_id="ChEBI:CHEBI:29105"; /ligand_label="2"; /evidence="ECO:0000256|PIRSR:PIRSR601952-2"; BINDING 379; /ligand="Zn(2+)"; /ligand_id="ChEBI:CHEBI:29105"; /ligand_label="2"; /evidence="ECO:0000256|PIRSR:PIRSR601952-2"; BINDING 454; /ligand="Zn(2+)"; /ligand_id="ChEBI:CHEBI:29105"; /ligand_label="2"; /evidence="ECO:0000256|PIRSR:PIRSR601952-2"
Subellular location
Cell membrane ; Lipid-anchor, GPI-anchor. Membrane ; Lipid-anchor, GPI-anchor .
Structure
Homodimer.
Target Relevance information above includes information from UniProt accession: F1M8U7
The UniProt Consortium

HPLC of Rat Alkaline Phosphatase (Germ type) /ALPG Protein
The purity of Rat Alkaline Phosphatase (Germ type) is greater than 95% as determined by SEC-HPLC.
SDS-PAGE gel of Rat Alkaline Phosphatase (Germ type) /ALPG Protein
Rat Alkaline Phosphatase (Germ type) on Tris-Bis PAGE under reduced condition. The purity is greater than 95%.

Publications

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We haven't added any publications to our database yet.
Published literature highly relevant to the biological target of this product and referencing this antibody or clone are retrieved from PubMed database provided by The United States National Library of Medicine at the National Institutes of Health.

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