ALPL Protein (AA 18-501) (His tag)
Quick Overview for ALPL Protein (AA 18-501) (His tag) (ABIN7597451)
Target
See all ALPL ProteinsProtein Type
Origin
Source
Purity
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Protein Characteristics
- AA 18-501
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Purification tag / Conjugate
- This ALPL protein is labelled with His tag.
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Purpose
- Recombinant human ALPL Protein with C-terminal 10xHis tag
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Sequence
- ALPL(Leu18-Ser501) 10xHis tag
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Application Notes
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Extracellular Domain Proteins (ECD) can be used as:
- Immunogens for antibody drug development
- Reagents used for CAR-T positive cell monitoring
- Reagents for antibody screening and functional testing
- Reagents for antibody affinity measurement
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Comment
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The protein was made using HEK293 mammalian cell secretion expression system to ensure the close-to-native structures and post-translational modifications of the target protein.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Buffer
- Lyophilized from sterile PBS, pH 7.4. Normally 5 % – 8% trehalose is added as protectants before lyophilization.
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Storage
- -20 °C,-80 °C
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Storage Comment
- Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.
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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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HOPS, HPPA, HPPC, HPPI, HPPO, TNAP, TNALP, APTNAP, TNSALP, AP-TNAP, TNS-ALP
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] -
Molecular Weight
- predicted molecular mass of 54.7 kDa after removal of the signal peptide. The apparent molecular mass of ALPL-His is 55-70 kDa due to glycosylation.
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UniProt
- P05186
Target
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