Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Applications | Tested Dilution | Publications |
---|---|---|
Western Blot (WB) |
1:500-1:1,000 | View 5 publications 5 publications |
Immunohistochemistry (IHC) |
Assay-dependent | View 3 publications 3 publications |
Immunocytochemistry (ICC/IF) |
1:20-1:200 | View 2 publications 2 publications |
Immunoprecipitation (IP) |
0.5-4.0 µg | - |
Product Specifications | |
---|---|
Species Reactivity |
Human, Mouse |
Published species |
Human, Mouse |
Host/Isotype |
Rabbit / IgG |
Class |
Polyclonal |
Type |
Antibody |
Immunogen |
SIX1 Fusion Protein Ag1044 (1-284 aa encoded by BC008874) |
Conjugate |
Unconjugated |
Form |
Liquid |
Concentration |
0.3 mg/mL |
Purification |
Antigen affinity chromatography |
Storage buffer |
PBS, pH 7.3, with 50% glycerol |
Contains |
0.02% sodium azide |
Storage conditions |
-20°C |
Immunogen sequence: MSMLPSFGF TQEQVACVCE VLQQGGNLER LGRFLWSLPA CDHLHKNESV LKAKAVVAFH RGNFRELYKI LESHQFSPHN HPKLQQLWLK AHYVEAEKLC GRPLGAVGKY RVRRKFPLPR TIWDGEETSY CFKEKSRGVL REWYAHNPYP SPREKRELAE ATGLTTTQVS NWFKNRRQRD RAAEAKEREN TENNNSSSNK QNQLSPLEGG KPLMSSSEEE FSPPQSPDQN SVLLLQGNMG HARSSNYSLP GLTASQPSHG LQTHQHQLQD SLLGPLTSSL VDLGS (1-284 aa encoded by BC008874)
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).
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Homeobox protein SIX1; Sine oculis homeobox homolog 1; sine oculis-related homeobox 1 homolog
Gene Aliases: BB138287; BOS3; DFNA23; SIX1; TIP39
UniProt ID: (Human) Q15475, (Mouse) Q62231
Entrez Gene ID: (Human) 6495, (Mouse) 20471
Molecular Function:
homeodomain transcription factor
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