TTPA antibody (AA 82-108)

Catalog No. ABIN5537880

Product Details anti-TTPA Antibody

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

Binding Specificity: AA 82-108

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TTPA antibody is un-conjugated

Application: Western Blotting (WB)

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

Immunogen: This TTPA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 82-108 amino acids from the Central region of human TTPA.

Isotype: Ig Fraction

Application Details

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

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 TTPA

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

Alternative Name: TTPA (TTPA Products)

Synonyms: ATTP antibody, AVED antibody, TTP1 antibody, alphaTTP antibody, TTP antibody, alpha-TTP antibody, alpha tocopherol transfer protein antibody, tocopherol (alpha) transfer protein (ataxia (Friedreich-like) with vitamin E deficiency) antibody, tocopherol (alpha) transfer protein antibody, TTPA antibody, ttpa antibody, Ttpa antibody

Background: 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.

Molecular Weight: 32 kDa

Gene ID: 7274

UniProt: P49638