TBL2 antibody (N-Term)

Catalog No. ABIN2785515

The Rabbit Polyclonal anti-TBL2 antibody has been validated for WB. It is suitable to detect TBL2 in samples from Human, Mouse, Horse and Rabbit.

Quick Overview for TBL2 antibody (N-Term) (ABIN2785515)

Target: TBL2 (Transducin (Beta)-Like 2 (TBL2))

Reactivity: Human, Mouse, Horse, Rabbit

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TBL2 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-TBL2 Antibody

Binding Specificity: N-Term

Sequence: RSGRPACQKA NGFPPDKSSG SKKQKQYQRI RKEKPQQHNF THRLLAAALK

Predicted Reactivity: Horse: 86%, Human: 100%, Mouse: 85%, Rabbit: 86%

Characteristics: This is a rabbit polyclonal antibody against TBL2. It was validated on Western Blot using a cell lysate as a positive control.

Purification: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the N terminal region of human TBL2

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator.

Comment:

Antigen size: 447 AA

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handling Advice: Avoid repeated freeze-thaw cycles.

Storage: -20 °C

Storage Comment: 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.

Target Details for TBL2

Target: TBL2 (Transducin (Beta)-Like 2 (TBL2))

Alternative Name: TBL2

Background: 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

Molecular Weight: 49 kDa

Gene ID: 26608

NCBI Accession: NM_012453, NP_036585

UniProt: Q9Y4P3