TBL2 antibody (N-Term)

Catalog No. ABIN5534762

Product Details anti-TBL2 Antibody

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

Binding Specificity: AA 43-72, N-Term

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TBL2 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This TBL2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 43-72 amino acids from the N-terminal region of human TBL2.

Isotype: Ig Fraction

Application Details

Application Notes: For WB starting dilution is: 1:1000

For IHC-P starting dilution is: 1:10~50

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

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

Storage: 4 °C,-20 °C

Storage Comment: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Target Details for TBL2

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

Alternative Name: TBL2 (TBL2 Products)

Synonyms: wu:fa96f08 antibody, tbl2 antibody, MGC53692 antibody, TBL2 antibody, MGC79804 antibody, MGC140759 antibody, DKFZp469O1728 antibody, WBSCR13 antibody, WS-betaTRP antibody, C76179 antibody, WS-bTRP antibody, transducin (beta)-like 2 antibody, transducin (beta)-like 2 L homeolog antibody, transducin beta like 2 antibody, tbl2 antibody, tbl2.L antibody, TBL2 antibody, Tbl2 antibody

Background: 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.

Molecular Weight: 50 kDa

Gene ID: 26608

UniProt: Q9Y4P3