ADAMTS13 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)
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- Target See all ADAMTS13 Proteins
- ADAMTS13 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13))
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 1
- Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This ADAMTS13 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human ADAMTS13 (transcript variant 1) 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 ADAMTS13 Protein
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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
- ADAMTS13 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13))
- Alternative Name
- Adamts13 (ADAMTS13 Products)
- Synonyms
- ADAMTS13 Protein, ADAM-TS13 Protein, ADAMTS-13 Protein, C9orf8 Protein, VWFCP Protein, vWF-CP Protein, Gm710 Protein, ADAM metallopeptidase with thrombospondin type 1 motif 13 Protein, a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 13 Protein, ADAM metallopeptidase with thrombospondin type 1 motif, 13 Protein, ADAMTS13 Protein, Adamts13 Protein, adamts13 Protein
- Background
- This gene encodes a member of a family of proteins containing several distinct regions, including a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. The enzyme encoded by this gene specifically cleaves von Willebrand Factor (vWF). Defects in this gene are associated with thrombotic thrombocytopenic purpura. Alternative splicing results in multiple transcript variants.
- Molecular Weight
- 149.9 kDa
- NCBI Accession
- NP_620594
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