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ZBTB24 (基因名), Zinc finger and BTB domain-containing protein 24 (蛋白名), zbt24_human.
产品名称:

Human ZBTB24/ Zinc finger and BTB domain-containing protein 24 Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

Zinc finger protein 450, KIAA0441, ZNF450

序列号:
O43167
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 ZBTB24 Protein
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Human ZBTB24 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


基因位点
Cytogenetic band: 6q21 by HGNC 6q21 by Entrez Gene 6q21 by Ensembl
ZBTB24 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:
N/A


功能:
May be involved in BMP2-induced transcription.


亚细胞位置:
Nucleus


该产品尚未在任何出版物中被引用。

[1].
"Prediction of the coding sequences of unidentified human genes. VIII. 78 new cDNA clones from brain which code for large proteins in vitro."

[2].
"Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2."

[3].
"Many sequence variants affecting diversity of adult human height."

[4].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[5].
"The DNA sequence and analysis of human chromosome 6."

[6].
"Construction of expression-ready cDNA clones for KIAA genes: manual curation of 330 KIAA cDNA clones."

[7].
"Roles of Alternative RNA Splicing of the Bif-1 Gene by SRRM4 During the Development of Treatment-induced Neuroendocrine Prostate Cancer."

[8].
"Comparative methylome analysis of ICF patients identifies heterochromatin loci that require ZBTB24, CDCA7 and HELLS for their methylated state."

[9].
"Architecture of the human interactome defines protein communities and disease networks."

[10].
"Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2."
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