Human Alkaline Phosphatase, Liver/Bone/Kidney (ALPL) ELISA Kit (96T)

Human Alkaline Phosphatase, Liver/Bone/Kidney (ALPL) ELISA Kit (96T)

Catalog #: TD1846
Availability: In Stock
¥619.00
Detection range: 78.1-5000pg/mL    
Sensitivity: 36pg/mL    
Type: Traditional ALPL ELISA kit    
Synonyms: BALP; BSAP; HOPS; AP-TNAP; TNSALP; Bone Alkaline Phosphatase; Alkaline Phosphatase,Tissue-Nonspecific Isozyme
Species: Human
Sample type: serum, plasma or other biological fluids.
Experimental method: Sandwich
Shelf life: 12 months
Gene ID: 249
UniProt ID: P05186
Component: 1. Pre-coated, ready to use 96-well strip plate 1
2. Plate sealer for 96 wells 2
3. Standard 2
4. Diluents buffer: 1×45 mL
5. Detection Reagent A: 1×120 μL
6. Detection Reagent B: 1×120 μL
7. TMB Substrate: 1×9 mL
8. Stop Solution: 1×6 mL
9. Wash Buffer (30× concentrate): 1×20 mL




Background

The gene ALPL 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.

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ALPL