WBSCR22 Antikörper (Center)
Kurzübersicht für WBSCR22 Antikörper (Center) (ABIN2856201)
Target
Alle WBSCR22 Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- Center
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Produktmerkmale
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Rabbit Polyclonal antibody to WBSCR22 (Williams Beuren syndrome chromosome region 22)
WBSCR22 antibody -
Aufreinigung
- Purified by antigen-affinity chromatography.
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Immunogen
- Recombinant protein encompassing a sequence within the center region of human WBSCR22. The exact sequence is proprietary.
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Isotyp
- IgG
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Applikationshinweise
- Suggested dilution Reference ICC/IF 1:100-1:1000* IHC (Formalin-fixed paraffin-embedded sections) 1:100-1:1000* Immunoprecipitation 1:500-1:1000* Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceICC/IF1:100-1:1000* IHC (Formalin-fixed paraffin-embedded sections)1:100-1:1000* Immunoprecipitation1:500-1:1000* Western blot1:500-1:3000*
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Kommentare
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Positive Control: HeLa , HCT116 , *A375M ,
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 0.42 mg/mL
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Buffer
- 0.1M Tris, 0.1M Glycine, 10 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.
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Konservierungsmittel
- Thimerosal (Merthiolate)
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Vorsichtsmaßnahmen
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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Cardiac mitochondrial function depends on BUD23 mediated ribosome programming." in: eLife, Vol. 9, (2020) (PubMed).
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Cardiac mitochondrial function depends on BUD23 mediated ribosome programming." in: eLife, Vol. 9, (2020) (PubMed).
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- WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
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Andere Bezeichnung
- WBSCR22
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Hintergrund
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This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
Cellular Localization: Nucleus -
Molekulargewicht
- 32 kDa
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Gen-ID
- 114049
Target
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