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首页  >  重组蛋白  >  Human ABCD2 Recombinant Protein
ABCD2 (基因名), ATP-binding cassette sub-family D member 2 (蛋白名), ABCD2_HUMAN.
产品名称:

Human ABCD2/ ATP-binding cassette sub-family D member 2 Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

Adrenoleukodystrophy-like 1, Adrenoleukodystrophy-related protein, hALDR, ALD1, ALDL1, ALDR, ALDRP

序列号:
Q9UBJ2
来源:
E.coli
种属:
Human
标签:
His
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
-
Human ABCD2 Protein
×
Human ABCD2 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


基因位点
Cytogenetic band: 12q12 by HGNC 12q12 by Entrez Gene 12q12 by Ensembl
ABCD2 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
Can form heterodimers with ABCD1/ALD and ABCD3/PMP70. Dimerization is necessary to form an active transporter. Interacts with PEX19.


功能:
Probable transporter.


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].
"A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression pattern."

[2].
"Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19p."

[3].
"Full length cDNA cloning, promoter sequence, and genomic organization of the human adrenoleukodystrophy related (ALDR) gene functionally redundant to the gene responsible for X-linked adrenoleukodystrophy."

[4].
"cDNA cloning and mRNA expression of the human adrenoleukodystrophy related protein (ALDRP), a peroxisomal ABC transporter."

[5].
"Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression."

[6].
"Association study between single-nucleotide polymorphisms in 199 drug-related genes and commonly measured quantitative traits of 752 healthy Japanese subjects."

[7].
"Multiple genetic variants along candidate pathways influence plasma high-density lipoprotein cholesterol concentrations."

[8].
"X-linked adrenoleukodystrophy phenotype is independent of ABCD2 genotype."

[9].
"Effect of testosterone metabolites on ABC half-transporter relative gene expression in X-linked adrenoleukodystrophy."

[10].
"Liver X receptor alpha interferes with SREBP1c-mediated Abcd2 expression. Novel cross-talk in gene regulation."
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