SIX Homeobox 1 Antikörper
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- Target Alle SIX Homeobox 1 (SIX1) Antikörper anzeigen
- SIX Homeobox 1 (SIX1)
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser SIX Homeobox 1 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), ELISA
- Aufreinigung
- Antibody is purified by peptide affinity chromatography method.
- Immunogen
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SIX1.
- Top Product
- Discover our top product SIX1 Primärantikörper
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- Applikationshinweise
- 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.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Lyophilized
- Rekonstitution
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- Konzentration
- 1 mg/mL
- Buffer
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- Handhabung
- As with any antibody avoid repeat freeze-thaw cycles.
- Lagerung
- 4 °C/-20 °C
- Informationen zur Lagerung
- 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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- Target
- SIX Homeobox 1 (SIX1)
- Andere Bezeichnung
- SIX1 (SIX1 Produkte)
- Synonyme
- BOS3 antikoerper, DFNA23 antikoerper, TIP39 antikoerper, BB138287 antikoerper, six1b antikoerper, six2 antikoerper, zgc:92332 antikoerper, XSix1 antikoerper, six1 antikoerper, zgc:77345 antikoerper, SIX homeobox 1 antikoerper, sine oculis-related homeobox 1 antikoerper, SIX homeobox 1a antikoerper, SIX homeobox 1 L homeolog antikoerper, SIX homeobox 1b antikoerper, SIX1 antikoerper, Six1 antikoerper, six1a antikoerper, six1.L antikoerper, six1b antikoerper
- Hintergrund
- 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.
- Molekulargewicht
- 32 kDa
- Gen-ID
- 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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