FAM136A Protein (Myc-DYKDDDDK Tag)
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- Target Alle FAM136A Proteine anzeigen
- FAM136A (Family with Sequence Similarity 136, Member A (FAM136A))
- Protein-Typ
- Recombinant
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Spezies
- Human
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Quelle
- HEK-293 Cells
- Aufreinigungstag / Konjugat
- Dieses FAM136A Protein ist gelabelt mit Myc-DYKDDDDK Tag.
- Applikation
- Antibody Production (AbP), Standard (STD)
- Produktmerkmale
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- Recombinant human FAM136A protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Reinheit
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product FAM136A Protein
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- Applikationshinweise
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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 - Kommentare
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The tag is located at the C-terminal.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Konzentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Lagerung
- -80 °C
- Informationen zur Lagerung
- 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
- FAM136A (Family with Sequence Similarity 136, Member A (FAM136A))
- Andere Bezeichnung
- Fam136a (FAM136A Produkte)
- Synonyme
- 2010309E21Rik Protein, AW124904 Protein, Hyccin Protein, RGD1304825 Protein, ik:tdsubc_1a11 Protein, wu:fb72f05 Protein, xx:tdsubc_1a11 Protein, zgc:73247 Protein, family with sequence similarity 136 member A Protein, family with sequence similarity 136, member A Protein, family with sequence similarity 136 member A S homeolog Protein, FAM136A Protein, Fam136a Protein, fam136a.S Protein, fam136a Protein
- Hintergrund
- This gene encodes a mitochondrially localized protein that is highly conserved across species. The gene is expressed in a variety of tissues including human lymphoblast cells and rat neurosensorial epithelium of the cristaampullaris. A mutation in this gene has been associated with familial Meniere's disease, a chronic disorder of the inner ear. Several pseudogenes of this gene are found on other chromosomes. Alternative splicing results in multiple transcript variants.
- Molekulargewicht
- 15.5 kDa
- NCBI Accession
- NP_116211
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