TBL2 Antikörper (N-Term)
Kurzübersicht für TBL2 Antikörper (N-Term) (ABIN2785515)
Target
Alle TBL2 Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- N-Term
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Sequenz
- RSGRPACQKA NGFPPDKSSG SKKQKQYQRI RKEKPQQHNF THRLLAAALK
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Homologie
- Horse: 86%, Human: 100%, Mouse: 85%, Rabbit: 86%
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Produktmerkmale
- This is a rabbit polyclonal antibody against TBL2. It was validated on Western Blot using a cell lysate as a positive control.
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Aufreinigung
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the N terminal region of human TBL2
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Applikationshinweise
- Optimal working dilutions should be determined experimentally by the investigator.
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Kommentare
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Antigen size: 447 AA
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- Lot specific
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Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handhabung
- Avoid repeated freeze-thaw cycles.
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Lagerung
- -20 °C
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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.
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- TBL2 (Transducin (Beta)-Like 2 (TBL2))
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Andere Bezeichnung
- TBL2
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Hintergrund
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TBL2 is a member of the beta-transducin protein family. Most proteins of the beta-transducin family are involved in regulatory functions. This protein is possibly involved in some intracellular signaling pathway. 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 beta-transducin protein family. Most proteins of the beta-transducin family are involved in regulatory functions. This protein is possibly involved in some intracellular signaling pathway. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.
Alias Symbols: DKFZP43N024, MGC134739, WBSCR13, WS-betaTRP
Protein Interaction Partner: UBC, SUMO1, SUZ12, RNF2, ESR1, MRPL53, SARNP, SUGP1, CDV3, RBM27, SF3B4, SOD2, SCP2, RPS19, NDUFA7, NDUFA2, SERPINH1, UBD, GRK5, COPS5, CUL3, PDPK1, USP44,
Protein Size: 447 -
Molekulargewicht
- 49 kDa
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Gen-ID
- 26608
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NCBI Accession
- NM_012453, NP_036585
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UniProt
- Q9Y4P3
Target
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