Alkalinefosfatase (ALPL) Mouse Monoclonal Antibody [Kloon ID: LBI3A1]

This gene encodes a member of the alkaline phosphatase family of proteins. There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific) . The first three are located together on chromosome 2, while the tissue non-specific form is located on chromosome 1. The product of this gene is a membrane bound glycosylated enzyme that is not expressed in any particular tissue and is, therefore, referred to as the tissue-nonspecific form of the enzyme. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature enzyme. This enzyme may play a role in bone mineralization. Mutations in this gene have been linked to hypophosphatasia, a disorder that is characterized by hypercalcemia and skeletal defects. [provided by RefSeq, Oct 2015]

Carrier-free (BSA/glycerol-free) ALPL mouse monoclonal antibody, clone LBI3A1

AP-TNAP; APTNAP; HOPS; TNAP; TNSALP

Homo sapiens alkaline phosphatase, biomineralization associated (ALPL), transcript variant 1, mRNA.

249

P05186

Unconjugated

Folate biosynthesis, Metabolic pathways

Folate biosynthesis, Metabolic pathways

WB 1:2000

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Druggable Genome

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

ALPL

https://www.ncbi.nlm.nih.gov/gene/?term=249

https://www.uniprot.org/uniprot/P05186