SIX Homeobox 1 Protein (SIX1) (His tag)
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- Target Alle SIX Homeobox 1 (SIX1) Proteine anzeigen
- SIX Homeobox 1 (SIX1)
- Protein-Typ
- Recombinant
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Spezies
- Human
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Quelle
- Escherichia coli (E. coli)
- Aufreinigungstag / Konjugat
- Dieses SIX Homeobox 1 Protein ist gelabelt mit His tag.
- Applikation
- Antibody Production (AbP), Standard (STD)
- Produktmerkmale
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- Recombinant human Purified recombinant protein of Human SIX homeobox 1 (SIX1), full length, with N-terminal HIS tag, expressed in E. coli, 50 μg (full length, N-term HIS tag) protein expressed in E.coli.
- Produced with end-sequenced ORF clone
- Aufreinigung
- Purified
- Reinheit
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product SIX1 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 N-terminal.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Konzentration
- 50 μg/mL
- Buffer
- 25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.
- 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
- SIX Homeobox 1 (SIX1)
- Andere Bezeichnung
- SIX homeobox 1 (SIX1 Produkte)
- Synonyme
- BOS3 Protein, DFNA23 Protein, TIP39 Protein, BB138287 Protein, six1b Protein, six2 Protein, zgc:92332 Protein, XSix1 Protein, six1 Protein, zgc:77345 Protein, SIX homeobox 1 Protein, sine oculis-related homeobox 1 Protein, SIX homeobox 1a Protein, SIX homeobox 1 L homeolog Protein, SIX homeobox 1b Protein, SIX1 Protein, Six1 Protein, six1a Protein, six1.L Protein, six1b Protein
- Hintergrund
- The protein encoded by this gene is a homeobox protein that is similar to the Drosophila 'sine oculis' gene product. This gene is found in a cluster of related genes on chromosome 14 and is thought to be involved in limb development. Defects in this gene are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3).
- Molekulargewicht
- 32 kDa
- NCBI Accession
- NP_005973
- Pathways
- Sensory Perception of Sound, Regulation of Muscle Cell Differentiation, Tube Formation, Skeletal Muscle Fiber Development
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