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  • Íÿ¹ABCD2¶à¿Ë¡¿¹Ìå

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ÖÐÎÄÃû³Æ£º Íÿ¹ABCD2¶à¿Ë¡¿¹Ìå

Ó¢ÎÄÃû³Æ£º Anti-ABCD2 rabbit polyclonal antibody

±ð      Ãû£º ALDR; ABC39; ALDL1; ALDRP; hALDR

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´¢      ´æ£º Àä¶³£¨-20¡æ£©

ËÞ      Ö÷£º Rabbit

¿¹      Ô­£º ABCD2

·´Ó¦ÖÖÊô£º Human, Mouse, Rat

±ê ¼Ç Î Unconjugate

¿Ë¡ÀàÐÍ£º rabbit polyclonal

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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.

Applications:

ELISA, IHC

Name of antibody:

ABCD2

Immunogen:

Synthetic peptide of human ABCD2

Full name:

ATP-binding cassette, sub-family D (ALD), member 2

Synonyms£º

ALDR; ABC39; ALDL1; ALDRP; hALDR

SwissProt:

Q9UBJ2

ELISA Recommended dilution:

2000-5000

IHC positive control:

Human ovarian cancer and Human thyroid cancer

IHC Recommend dilution:

25-100




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