TBL2 antibody (N-Term)

Catalog No. ABIN656760

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.

Clone: RB32541

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000. IHC-P: 1:10~50

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody 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: TBL2 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Expiry Date: 6 months

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: 49798

Gene ID: 26608

NCBI Accession: NP_036585

UniProt: Q9Y4P3