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Rabbit polyclonal to TTPA
Synthetic peptide conjugated to KLH, corresponding to a region within internal sequence amino acids 82-108 of Human TTPA (NP_000361.1).
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Store at -20°C long term.
Preservative: 0.09% Sodium azide
Constituent: 99% PBS
Concentration information loading...
Immunogen affinity purified
ab156208 is purified through a protein A column, followed by peptide affinity purification.
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in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
1/100 - 1/500. Predicted molecular weight: 32 kDa.
Binds alpha-tocopherol and enhances its transfer between separate membranes.
Involvement in disease
Defects in TTPA are the cause of ataxia with isolated vitamin E deficiency (AVED) [MIM:277460]. AVED is an autosomal recessive disease characterized by spinocerebellar degeneration. It causes ataxia and peripheral neuropathy that resembles Friedreich ataxia. AVED patients have markedly reduced plasma levels of vitamin E.
Contains 1 CRAL-TRIO domain.
Information by UniProt
Alpha-tocopherol transfer protein antibody
has not yet been referenced specifically in any publications.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"