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PEX10 (基因名), Peroxisome biogenesis factor 10 (蛋白名), PEX10_HUMAN.
产品名称:

Human PEX10/ Peroxisome biogenesis factor 10 Peptide

货号:

-

监管等级:
商标:
EIAab®
种属:
Human
形态:
Lyophilized powder
表征:
The peptide is characterized by mass spectroscopy
溶液澄清度:
In DMSO clear solution
Human PEX10 Peptide
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Human PEX10 Peptide
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该产品尚未在任何出版物中被引用。

[1].
"Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders."

[2].
"Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders."

[3].
"Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B."

[4].
"A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia."

[5].
"The DNA sequence and biological annotation of human chromosome 1."

[6].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[7].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[8].
"Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene."

[9].
"Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences."

[10].
"PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis."
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