BAZ1B Antikörper (Middle Region)
Kurzübersicht für BAZ1B Antikörper (Middle Region) (ABIN2781194)
Target
Alle BAZ1B Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
-
-
Bindungsspezifität
- Middle Region
-
Sequenz
- EQCLVALLHK HLPGHPYVRR KRKKFPDRLA EDEGDSEPEA VGQSRGRRQK
-
Homologie
- Cow: 93%, Dog: 86%, Guinea Pig: 86%, Horse: 86%, Human: 100%, Mouse: 79%, Pig: 93%, Rat: 79%
-
Produktmerkmale
- This is a rabbit polyclonal antibody against BAZ1B. It was validated on Western Blot using a cell lysate as a positive control.
-
Aufreinigung
- Affinity Purified
-
Immunogen
- The immunogen is a synthetic peptide directed towards the middle region of human BAZ1B
-
-
-
-
Applikationshinweise
- Optimal working dilutions should be determined experimentally by the investigator.
-
Kommentare
-
Antigen size: 1483 AA
-
Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
-
-
Format
- Liquid
-
Konzentration
- Lot specific
-
Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
-
Konservierungsmittel
- Sodium azide
-
Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
-
Handhabung
- Avoid repeated freeze-thaw cycles.
-
Lagerung
- -20 °C
-
Informationen zur Lagerung
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
-
-
- BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
-
Andere Bezeichnung
- BAZ1B
-
Hintergrund
-
BAZ1B is 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.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. 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.
Alias Symbols: WBSCR10, WBSCR9, WSTF
Protein Interaction Partner: VDR, TOP2B, SMARCC2, SMARCC1, HIST1H3A, UBC, EED, RNF2, NR4A2, LMNA, HDAC11, WHSC1, MBD3, SRRM2, SMARCA5, SMARCD2, SMARCA4, SIRT7, SUMO2, HDGF, SUMO1, tat, PCNA, SIN3A, NCOR1, HIST1H4A, HIST2H2BE, HIST2H2AC, TCF3, HDAC2, DEK, RHD, MYO1C, MYBBP1A, SF3B1, E
Protein Size: 1483 -
Molekulargewicht
- 171 kDa
-
Gen-ID
- 9031
-
NCBI Accession
- NM_032408, NP_115784
-
UniProt
- Q9UIG0
-
Pathways
- Nuclear Hormone Receptor Binding, Chromatin Binding
Target
-