TTPA antibody (C-Term)

Catalog No. ABIN7466358

This Rabbit Polyclonal antibody specifically detects TTPA in WB, ICC, IF and IHC (p). It exhibits reactivity toward Human.

Quick Overview for TTPA antibody (C-Term) (ABIN7466358)

Target: TTPA (Tocopherol (Alpha) Transfer Protein (TTPA))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TTPA antibody is un-conjugated

Application: Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-TTPA Antibody

Binding Specificity: C-Term

Cross-Reactivity: Hamster, Human, Mouse, Rat

Purification: Purified by antigen-affinity chromatography.

Immunogen: Carrier-protein conjugated synthetic peptide encompassing a sequence within the C-terminus region of human alpha TTP. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: IMR32 , mouse liver , rat liver

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for TTPA

Target: TTPA (Tocopherol (Alpha) Transfer Protein (TTPA))

Alternative Name: alpha tocopherol transfer protein

Background: Alpha tocopherol transfer protein , ATTP , AVED , TTP1 , alphaTTP,This gene encodes a soluble protein that binds alpha-trocopherol, a form of vitamin E, with high selectivity and affinity. This protein plays an important role in regulating vitamin E levels in the body by transporting vitamin E between membrane vesicles and facilitating the secretion of vitamin E from hepatocytes to circulating lipoproteins. Mutations in this gene cause hereditary vitamin E deficiency (ataxia with vitamin E deficiency, AVED) and retinitis pigmentosa. [provided by RefSeq]

Molecular Weight: 32 kDa

Gene ID: 7274

UniProt: P49638