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首页  >  酶联免疫试剂盒  >  Human ABCD1 ELISA Kit
ABCD1 (基因名), ATP-binding cassette sub-family D member 1 (蛋白名), ABCD1_HUMAN.
产品名称:

Human ABCD1/ ATP-binding cassette sub-family D member 1 ELISA Kit

货号:
-
商标:
EIAab®
监管等级:
别名:

Adrenoleukodystrophy protein, ALDP, ALD

检测方法:
ELISA
特异性:
Natural and recombinant human ATP-binding cassette sub-family D member 1
样品类型:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
样品数据:
研究领域:
Cardiovascular
Human ABCD1 ELISA Kit
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Human ABCD1 ELISA Kit
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产品说明书


通用注释


亚单元:
Can form homodimers and heterodimers with ABCD2/ALDR and ABCD3/PMP70. Dimerization is necessary to form an active transporter. Interacts with PEX19.


功能:
Probable transporter. The nucleotide-binding fold acts as an ATP-binding subunit with ATPase activity.


亚细胞位置:
Peroxisome membrane Multi-pass membrane protein


该产品尚未在任何出版物中被引用。

[1].
"Live cell FRET microscopy: homo- and heterodimerization of two human peroxisomal ABC transporters, the adrenoleukodystrophy protein (ALDP, ABCD1) and PMP70 (ABCD3)."

[2].
"ATP-binding and -hydrolysis activities of ALDP (ABCD1) and ALDRP (ABCD2), human peroxisomal ABC proteins, overexpressed in Sf21 cells."

[3].
"Function of the PEX19-binding site of human adrenoleukodystrophy protein as targeting motif in man and yeast. PMP targeting is evolutionarily conserved."

[4].
"Probing substrate-induced conformational alterations in adrenoleukodystrophy protein by proteolysis."

[5].
"Identification of seven novel mutations in ABCD1 by a DHPLC-based assay in Italian patients with X-linked adrenoleukodystrophy."

[6].
"Live cell FRET microscopy: homo- and heterodimerization of two human peroxisomal ABC transporters, the adrenoleukodystrophy protein (ALDP, ABCD1) and PMP70 (ABCD3)."

[7].
"ATP-binding and -hydrolysis activities of ALDP (ABCD1) and ALDRP (ABCD2), human peroxisomal ABC proteins, overexpressed in Sf21 cells."

[8].
"Function of the PEX19-binding site of human adrenoleukodystrophy protein as targeting motif in man and yeast. PMP targeting is evolutionarily conserved."

[9].
"Probing substrate-induced conformational alterations in adrenoleukodystrophy protein by proteolysis."

[10].
"Identification of seven novel mutations in ABCD1 by a DHPLC-based assay in Italian patients with X-linked adrenoleukodystrophy."
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