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  • 產(chǎn)品名稱：ZCCHC9 抗原（重組蛋白）

  • 產(chǎn)品型號(hào)：100ug
  • 產(chǎn)品廠商：通蔚生物
  • 產(chǎn)品價(jià)格：800
  • 產(chǎn)品庫(kù)存：35
  • 產(chǎn)品文檔：
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ZCCHC9 抗原（重組蛋白）奉行以人為本、唯才善用，提倡人是核心資本，公平合理并創(chuàng)造性地使用人才，盡可能的給員工提供足夠的舞臺(tái)去發(fā)揮去成長(zhǎng)，公司尊重人，尊重每一位員工的個(gè)性，依托這樣的人才觀，將進(jìn)一步完善科學(xué)合理的人力資源管理機(jī)制，造就一個(gè)良好的人才成長(zhǎng)空間。
詳情介紹：

中文名稱： ZCCHC9 抗原（重組蛋白）

英文名稱： ZCCHC9 Antigen (Recombinant Protein)

別     名：  zinc finger, CCHC domain containing 9; PPP1R41

儲(chǔ)     存：  冷凍（-20℃）

相關(guān)類別： 抗原

概     述

Fusion protein corresponding to C terminal 200 amino acids of human ZCCHC9

技術(shù)規(guī)格

Full name:

zinc finger, CCHC domain containing 9

Synonyms:

PPP1R41

Swissprot:

Q8N567

Gene Accession:

BC032736

Purity:

>85%, as determined by Coomassie blue stained SDS-PAGE

Expression system:

Escherichia coli

Tags:

His tag C-Terminus, GST tag N-Terminus

Background:

Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. ZCCHC9 (zinc finger, CCHC domain containing 9) is a 271 amino acid protein that contains four CCHC-type zinc finger, suggesting a role in transcriptional regulation. The gene encoding ZCCHC9 maps to human chromosome 5, which contains 181 million base pairs and comprises nearly 6% of the human genome. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5-associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.






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