CDH23 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)
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- Target Alle CDH23 Proteine anzeigen
- CDH23 (Cadherin 23 (CDH23))
- Protein-Typ
- Recombinant
- Proteineigenschaft
- Transcript Variant 2
- Spezies
- Human
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Quelle
- HEK-293 Cells
- Aufreinigungstag / Konjugat
- Dieses CDH23 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
- Applikation
- Antibody Production (AbP), Standard (STD)
- Produktmerkmale
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- Recombinant human Cadherin-23 (transcript variant 2) 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 CDH23 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
- CDH23 (Cadherin 23 (CDH23))
- Andere Bezeichnung
- Cadherin-23 (CDH23 Produkte)
- Synonyme
- 4930542A03Rik Protein, USH1D Protein, ahl Protein, ahl1 Protein, bob Protein, bus Protein, mdfw Protein, nmf112 Protein, nmf181 Protein, nmf252 Protein, sals Protein, v Protein, CDHR23 Protein, W Protein, cadherin 23 (otocadherin) Protein, cadherin related 23 Protein, cadherin-related 23 Protein, Cdh23 Protein, CDH23 Protein
- Hintergrund
- This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Upregulation of this gene may also be associated with breast cancer. Alternative splice variants encoding different isoforms have been described.
- Molekulargewicht
- 58.4 kDa
- NCBI Accession
- NP_443068
- Pathways
- Sensory Perception of Sound
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