Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70 °C as supplied.
1 month, 2 to 8 °C under sterile conditions after reconstitution.
6 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.
Preservative
No Preservative
Concentration
LYOPH
Reconstitution Instructions
Reconstitute at 0.5 mg/mL in sterile PBS.
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Alkaline Phosphatase/ALPL Antibody (388816) [Unconjugated]
Akp2
Alkaline phosphatase liver/bone/kidney isozyme
alkaline phosphatase, liver/bone/kidney
alkaline phosphatase, tissue-nonspecific isozyme
alkaline phosphomonoesterase
ALPL
APTNAP
AP-TNAP
EC 3.1.3.1
FLJ40094
FLJ93059
glycerophosphatase
HOPS
liver/bone/kidney-type alkaline phosphatase
MGC161443
tissue-nonspecific ALP
TNAP
TNSALP
TNSALPMGC167935
Background
Four distinct genes encode alkaline phosphatases (APs) in humans (1). The ALPL gene encodes the liver/bone/kidney isozyme, also known as the tissue-nonspecific AP (TNAP). In comparison, ALPI, ALPP and ALPPL2 encode intestinal, placental and placental-like or germ cell APs, respectively. The serum levels of human APs are useful tumor markers (2). There are many mutations in the ALPL gene, leading to different forms of hypophosphatasia, characterized by poorly mineralized cartilage and bones (3). The native ALPL is a glycosylated homodimer attached to the membrane through a GPI-anchor. The C-terminal pro peptide (residues 503‑524) is not present in the mature form.
Le Du, M-H. and J.L. Millan (2002) J. Biol. Chem. 277:49808.
Di Mauro, S. et al. (2002) J. Bone Miner. Res. 17:1383.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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