SIX Homeobox 1 (SIX1) (Middle Region) Peptide
SIX1
Reactivity: Human
Host: Synthetic
BP, WB
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- Target See all SIX Homeobox 1 (SIX1) products
- SIX Homeobox 1 (SIX1)
- Protein Region
- Middle Region
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-SIX1 antibody (Catalog #: ARP32375_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- SIX Homeobox 1 (SIX1)
- Synonyms
- BOS3 Peptide, DFNA23 Peptide, TIP39 Peptide, BB138287 Peptide, six1b Peptide, six2 Peptide, zgc:92332 Peptide, XSix1 Peptide, six1 Peptide, zgc:77345 Peptide, SIX homeobox 1 Peptide, sine oculis-related homeobox 1 Peptide, SIX homeobox 1a Peptide, SIX homeobox 1 L homeolog Peptide, SIX homeobox 1b Peptide, SIX1 Peptide, Six1 Peptide, six1a Peptide, six1.L Peptide, six1b Peptide
- Background
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SIX1 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).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). Sequence Note: This RefSeq record was created from transcript and genomic sequence data because no single transcript was available for the full length of the gene. The extent of this transcript is supported by transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: BOS3, DFNA23, TIP39
Protein Interaction Partner: AES,TLE1,AES,CCDC85B,DACH1,EYA1,EYA2,EYA3,EYA4,MDFI,SIX1,TLE1,CCDC85B,EYA1,EYA2,MDFI
Protein Size: 284 - Molecular Weight
- 32 kDa
- Gene ID
- 6495
- NCBI Accession
- NM_005982, NP_005973
- UniProt
- Q15475
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