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PHLDA2 (基因名), Pleckstrin homology-like domain family A member 2 (蛋白名), PHLA2_HUMAN.
产品名称:

Human PHLDA2/ Pleckstrin homology-like domain family A member 2 Peptide

货号:

SR0401h

监管等级:
商标:
EIAab®
种属:
Human
序列:
预估分子量:
17kDa (monomer)
应用:
WB
形态:
Lyophilized powder
表征:
The peptide is characterized by mass spectroscopy
溶液澄清度:
In DMSO clear solution
Human PHLDA2 Peptide
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Human PHLDA2 Peptide
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R&D 技术数据
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该产品尚未在任何出版物中被引用。

[1].
"Hypoxia regulates the expression of PHLDA2 in primary term human trophoblasts."

[2].
"The product of the imprinted gene IPL marks human villous cytotrophoblast and is lost in complete hydatidiform mole."

[3].
"Retention of imprinting of the human apoptosis-related gene TSSC3 in human brain tumors."

[4].
"A novel pleckstrin homology-related gene family defined by Ipl/Tssc3, TDAG51, and Tih1: tissue-specific expression, chromosomal location, and parental imprinting."

[5].
"Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples."

[6].
"The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis."

[7].
"A 2.5-Mb transcript map of a tumor-suppressing subchromosomal transferable fragment from 11p15.5, and isolation and sequence analysis of three novel genes."

[8].
"Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels."

[9].
"Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight."

[10].
"Upregulation of PHLDA2 in Dicer knockdown HEK293 cells."
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