ABCD1
Reactivity: Human
WB
Host: Rabbit
Polyclonal
unconjugated
Application Notes
Peptide ELISA: Antibody Detection Limit Dilution: 1/32000. Western Blot: Preliminary experiments gave an approx.50 kDa band in Human Brain(Cerebellum) lysates after 1 μg/mL antibody staining. Please note that currently we cannotfind an explanation in the literature for the band we observe given the calculated size of82.0 kDa according to NP_000024.2. The 50 kDa band was successfully blocked byincubation with the immunizing peptide. Other applications not tested. Optimal dilutions are dependent on conditions and should be determined by the user.
Restrictions
For Research Use only
Concentration
0.5 mg/mL
Buffer
Tris saline, pH 7.3 containing 0.02 % Sodium Azide as preservative and 0.5 % BSA as stabilizer.
Preservative
Sodium azide
Precaution of Use
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handling Advice
Avoid repeated freezing and thawing.
Storage
4 °C/-20 °C
Storage Comment
Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at-20 °C for longer.
Target
ABCD1
(ATP-Binding Cassette, Sub-Family D (Ald), Member 1 (ABCD1))
ABC42 antibody, ALD antibody, ALDP antibody, AMN antibody, RGD1562128 antibody, zgc:172102 antibody, ABCD1 antibody, Ald antibody, Aldgh antibody, ATP binding cassette subfamily D member 1 antibody, ATP-binding cassette, sub-family D (ALD), member 1 antibody, ATP-binding cassette sub-family D member 1 antibody, ATP binding cassette subfamily D member 1 L homeolog antibody, ABCD1 antibody, Abcd1 antibody, abcd1 antibody, CpipJ_CPIJ013253 antibody, VDBG_05717 antibody, abcd1.L antibody
Background
ABCD1 belongs to the ALD subfamily, of the superfamily of ATP-binding cassette (ABC) transporters and is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. This peroxisomal membrane protein is likely involved in the peroxisomal transport or catabolism of very long chain fatty acids. Defects in this gene have been identified as the underlying cause of adrenoleukodystrophy, an X-chromosome recessively inherited demyelinating disorder of the nervous system.Synonyms: ATP-binding cassette sub-family D member 1