ALPL antibody (AA 201-250)
Quick Overview for ALPL antibody (AA 201-250) (ABIN1451976)
Target
See all ALPL AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 201-250
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Purpose
- TNAP Antibody
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Specificity
- TNAP Polyclonal Antibody detects endogenous levels of TNAP protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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Immunogen
- The antiserum was produced against synthesized peptide derived from human ALPL. AA range:201-250
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Isotype
- IgG
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Application Notes
- WB 1:500 - 1:2000. ELISA: 1:40000. Not yet tested in other applications.
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Store at -20°C/1 year
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Expiry Date
- 12 months
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- ALPL (Alkaline Phosphatase, Liver/bone/kidney (ALPL))
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Alternative Name
- ALPL
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Background
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Synonyms: ALPL, Alkaline phosphatase, tissue-nonspecific isozyme, AP-TNAP, TNSALP, Alkaline phosphatase liver/bone/kidney isozyme
Background: 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. [prov
Gene Name: ALPL
Protein Name: Alkaline phosphatase tissue-nonspecific isozyme
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Molecular Weight
- 57 kDa
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Gene ID
- 249
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OMIM
- 146300
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UniProt
- P05186
Target
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