ABCD2 Rabbit Polyclonal Antibody
CAT#: TA308846
Rabbit polyclonal antibody to ABCD2 (ATP-binding cassette, sub-family D (ALD), member 2)
Need it in bulk or conjugated?
Get a free quote
CNY 6,281.00
Cited in 1 publication. |
CNY 3,080.00
CNY 300.00
CNY 1,430.00
Specifications
Product Data | |
Applications | WB |
Recommend Dilution | WB:1:500-1:3000 |
Reactivity | Human, Mouse, Chicken, Rat |
Host | Rabbit |
Clonality | Polyclonal |
Immunogen | Recombinant fragment corresponding to a region within amino acids 338 and 588 of ABCD2 (Uniprot ID#Q9UBJ2) |
Formulation | 0.1M Tris, 0.1M Glycine, 10% Glycerol (pH7). 0.01% Thimerosal was added as a preservative. |
Concentration | lot specific |
Purification | Purified by antigen-affinity chromatography. |
Conjugation | Unconjugated |
Storage Condition | Store at -20°C as received. |
Predicted Protein Size | 83 kDa |
Gene Name | ATP binding cassette subfamily D member 2 |
Database Link | |
Background | 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. [provided by RefSeq] |
Synonyms | ABC39; ALDL1; ALDR; ALDRP; hALDR |
Note | Seq homology of immunogen across species: Mouse (94%), Chicken (85%), Rat (92%) |
Reference Data | |
Protein Families | Druggable Genome |
Protein Pathways | ABC transporters |
Citations (1)
The use of this Antibodies has been cited in the following citations: |
---|
Brain endothelial dysfunction in cerebral adrenoleukodystrophy
,Musolino, PL;Gong, Y;Snyder, JM;Jimenez, S;Lok, J;Lo, EH;Moser, AB;Grabowski, EF;Frosch, MP;Eichler, FS;,
Brain
,PubMed ID 26377633
[ABCD2]
|
Documents
Product Manuals |
FAQs |
SDS |
Resources
抗体相关资料 |