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ABCD1 (zeige ABCD1 ELISA Kits) and ABCD2 are involved in the transport of long and very long chain fatty acids (VLCFA) or their CoA-derivatives into peroxisomes with different substrate specificities, while ABCD3 (zeige ABCD3 ELISA Kits) is involved in the transport of branched chain acyl-CoA (zeige GNPAT ELISA Kits) into peroxisomes.ABCD4 is deduced to take part in the transport of vitamin B12 (zeige NDUFB3 ELISA Kits) from lysosomes into the cytosol.
13-cis (zeige CISH ELISA Kits)-retinoic acid induces ABCD2 expression in human monocytes/macrophages.
ABCD2 has a role, but not a strong one, in risk of early recurrent events after transient ischemic attack
results show that although patients with ABCD2 score greater than 4 were more likely to develop recurrent TIA/CVA in short term, those with lesser score still harbour a considerable risk for TIA/CVA
The transcriptional activity of the ABCD2 promoter was strongly increased by ectopic expression of beta-catenin (zeige CTNNB1 ELISA Kits) and TCF-4 (zeige TCF4 ELISA Kits).
LXRalpha (zeige NR1H3 ELISA Kits) is a negative modulator of Abcd2, acting through a novel regulatory mechanism involving overlapping SREBP and LXRalpha (zeige NR1H3 ELISA Kits) binding sites
Testosterone metabolites increased expression of ABCD2 mRNA in fibroblasts from X-linked adrenoleukodystrophy patients.
These findings are of particular importance for the attempt of pharmacological induction of ABCD2 as a possible therapeutic approach in X-linked adrenoleukodystrophy.
LDRP (ABCD2) interacts with both farnesylated wild-type and farnesylation-deficient mutant PEX19 (zeige PEX19 ELISA Kits). This interaction is mediated by amino acids 1-218 of ALDRP.
ALDRP interacts with PMP70 (zeige ABCD3 ELISA Kits). This interaction occurs via the ALDRP C-terminus [374-740] and the PMP70 (zeige ABCD3 ELISA Kits) C-terminus [338-659]. This interaction was demonstrated using human PMP70 (zeige ABCD3 ELISA Kits) and mouse ALDRP.
ABCD1 (zeige ABCD1 ELISA Kits) and its homolog ABCD2 exist mainly as homotetramers in the peroxisomal membrane
Abcd2 is a strong modifier of the metabolic impairments in peritoneal macrophages of ABCD1 (zeige ABCD1 ELISA Kits)-deficient mice
The absence of ABCD2 altered expression of gene clusters associated with lipid metabolism, including PPARalpha (zeige PPARA ELISA Kits) signaling.
ABCD2 is a sterol regulatory element binding protein (zeige CNBP ELISA Kits) target gene that is highly abundant in fat and opposes the accumulation of dietary lipids generally absent from the triglyceride storage pool within adipose tissue.
Evidence against the adrenoleukodystrophy-related gene acting as a modifier of X-adrenoleukodystrophy.
Abcd1 (zeige ABCD1 ELISA Kits) and Abcd2 gene silencing sensitizes astrocytes for inflammation and may have a role in X-adrenoleukodystrophy
ABCD2 plays a role in th degradation of long-chain saturated and omega9-monounsaturated fatty acids and in the synthesis of docosahexanoic acid.
The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which 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. The function of this peroxisomal membrane protein is unknown\; however this protein is speculated to function as a dimerization partner of ABCD1 and/or other peroxisomal ABC transporters. Mutations in this gene have been observed in patients with adrenoleukodystrophy, a severe demyelinating disease. This gene has been identified as a candidate for a modifier gene, accounting for the extreme variation among adrenoleukodystrophy phenotypes. This gene is also a candidate for a complement group of Zellweger syndrome, a genetically heterogeneous disorder of peroxisomal biogenesis.
ATP-binding cassette, sub-family D, member 2
, ATP-binding cassette, sub-family D (ALD), member 2
, ATP-binding cassette sub-family D member 2
, ATP-binding cassette sub-family D member 2-like
, adrenoleukodystrophy-like 1
, adrenoleukodystrophy-related protein
, adrenoleukodystrophy related