ASL Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)
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- Target See all ASL Proteins
- ASL (Argininosuccinate Lyase (ASL))
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 2
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This ASL protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human Arginosuccinase (transcript variant 2) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product ASL Protein
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Argininosuccinate Lyase (ASL) (AA 1-464) protein (GST tag)
ASL Origin: Human Host: Wheat germ Recombinant ELISA, WB, AA, AP
Argininosuccinate Lyase (ASL) (AA 1-464) protein (His tag)ASL Origin: Human Host: Escherichia coli (E. coli) Recombinant Greater than 95 % as determined by SDS-PAGE ELISA, WB
Argininosuccinate Lyase (ASL) (Transcript Variant 1) protein (Myc-DYKDDDDK Tag)ASL Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
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- Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Target
- ASL (Argininosuccinate Lyase (ASL))
- Alternative Name
- Arginosuccinase (ASL Products)
- Background
- This gene encodes a member of the lyase 1 family. The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency. A nontranscribed pseudogene is also located on the long arm of chromosome 22. Alternatively spliced transcript variants encoding different isoforms have been described.
- Molecular Weight
- 51.5 kDa
- NCBI Accession
- NP_000039
- Pathways
- Response to Growth Hormone Stimulus
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