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MPLKIP (基因名), M-phase-specific PLK1-interacting protein (蛋白名), MPLKI_HUMAN.
产品名称:

Human MPLKIP/ M-phase-specific PLK1-interacting protein Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

TTD non-photosensitive 1 protein, C7orf11, TTDN1

序列号:
Q8TAP9
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 MPLKIP Protein
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Human MPLKIP 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: 7p14.1 by HGNC 7p14.1 by Entrez Gene 7p14.1 by Ensembl
MPLKIP 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:
Interacts with PLK1; phosphorylation-dependent.


功能:
May play a role in maintenance of cell cycle integrity by regulating mitosis or cytokinesis.


亚细胞位置:
Nucleus Cytoplasm Cytoplasm Cytoskeleton Microtubule organizing center Centrosome The subcellular location is regulated during cell cycle. During interphase located in the nucleus. During mitosis located at the centrosome and dispersed in the cytoplasm. During telophase located in the midbody. Colocalizes with PLK1 at the centrosome in M phase.


该产品尚未在任何出版物中被引用。

[1].
"Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophy."

[2].
"Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome."

[3].
"Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: no obvious genotype-phenotype relationships."

[4].
"TTDN1 is a Plk1-interacting protein involved in maintenance of cell cycle integrity."

[5].
"Global, in vivo, and site-specific phosphorylation dynamics in signaling networks."

[6].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[7].
"Novel contiguous gene deletion in peruvian girl with Trichothiodystrophy type 4 and glutaric aciduria type 3."

[8].
"Architecture of the human interactome defines protein communities and disease networks."

[9].
"Mitral regurgitation as a phenotypic manifestation of nonphotosensitive trichothiodystrophy due to a splice variant in MPLKIP."

[10].
"Substrate-Trapped Interactors of PHD3 and FIH Cluster in Distinct Signaling Pathways."
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