SIX Homeobox 1 anticorps
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- Antigène Voir toutes SIX Homeobox 1 (SIX1) Anticorps
- SIX Homeobox 1 (SIX1)
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp SIX Homeobox 1 est non-conjugé
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Application
- Western Blotting (WB), ELISA
- Purification
- Antibody is purified by peptide affinity chromatography method.
- Immunogène
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SIX1.
- Top Product
- Discover our top product SIX1 Anticorps primaire
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- Indications d'application
- SIX1 antibody can be used for detection of SIX1 by ELISA at 1:1562500. SIX1 antibody can be used for detection of SIX1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- Concentration
- 1 mg/mL
- Buffer
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- Conseil sur la manipulation
- As with any antibody avoid repeat freeze-thaw cycles.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store SIX1 antibody at -20 °C.
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- Antigène
- SIX Homeobox 1 (SIX1)
- Autre désignation
- SIX1 (SIX1 Produits)
- Synonymes
- anticorps BOS3, anticorps DFNA23, anticorps TIP39, anticorps BB138287, anticorps six1b, anticorps six2, anticorps zgc:92332, anticorps XSix1, anticorps six1, anticorps zgc:77345, anticorps SIX homeobox 1, anticorps sine oculis-related homeobox 1, anticorps SIX homeobox 1a, anticorps SIX homeobox 1 L homeolog, anticorps SIX homeobox 1b, anticorps SIX1, anticorps Six1, anticorps six1a, anticorps six1.L, anticorps six1b
- Sujet
- 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.
- Poids moléculaire
- 32 kDa
- ID gène
- 6495
- NCBI Accession
- NP_005973
- UniProt
- Q15475
- Pathways
- Sensory Perception of Sound, Regulation of Muscle Cell Differentiation, Tube Formation, Skeletal Muscle Fiber Development
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