BAZ1B Antikörper
-
- Target Alle BAZ1B Antikörper anzeigen
- BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
-
Reaktivität
- Human, Maus, Ratte
-
Wirt
- Kaninchen
-
Klonalität
- Polyklonal
-
Konjugat
- Dieser BAZ1B Antikörper ist unkonjugiert
-
Applikation
- Western Blotting (WB), Immunohistochemistry (IHC)
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant protein of human BAZ1B
- Isotyp
- IgG
- Top Product
- Discover our top product BAZ1B Primärantikörper
-
-
- Applikationshinweise
- WB 1:500 - 1:2000 IHC 1:50 - 1:200
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- Konzentration
- 1 mg/mL
- Buffer
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
-
- Target
- BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
- Andere Bezeichnung
- BAZ1B (BAZ1B Produkte)
- Synonyme
- BAZ1B antikoerper, wstf antikoerper, wbscr9 antikoerper, wbscr10 antikoerper, LOC100220420 antikoerper, WBSCR10 antikoerper, WBSCR9 antikoerper, WSTF antikoerper, C87820 antikoerper, Wbscr9 antikoerper, fi60d02 antikoerper, im:7137554 antikoerper, wu:fi60d02 antikoerper, bromodomain adjacent to zinc finger domain 1B antikoerper, bromodomain adjacent to zinc finger domain, 1B antikoerper, bromodomain adjacent to zinc finger domain 1B S homeolog antikoerper, BAZ1B antikoerper, baz1b antikoerper, Baz1b antikoerper, baz1b.S antikoerper
- Hintergrund
-
Synonyms: Bromodomain Adjacent To Zinc Finger Domain 1B,Williams-Beuren Syndrome Chromosomal Region 10 Protein,Williams-Beuren Syndrome Chromosomal Region 9 Protein,Williams Syndrome Transcription Factor,Transcription Factor WSTF,EC 2.7.10.2,WBSCR10,WBSCR9.
Background: This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.
- Molekulargewicht
-
Observed_MW: 190kDa
Calculated_MW: 170kDa
- Gen-ID
- 9031
- UniProt
- Q9UIG0
- Pathways
- Nuclear Hormone Receptor Binding, Chromatin Binding
-