97久久久精品综合88久久_亚洲国产精品一_久热热国产久热_97操操操_北条麻妃在线免费观看_精品国自产拍天天拍

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯系我們
国产人妻人伦精品潘金莲,国产视频网站一区二区三区,无码精油按摩潮喷在播放
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-STIL/PE Conjugated antibody (bs-9303R-PE)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-9303R-PE
英文名稱 Rabbit Anti-STIL/PE Conjugated antibody
中文名稱 PE標記的中斷位點蛋白STIL抗體
別    名 MCPH7; SCL interrupting locus protein; SCL-interrupting locus protein; SCL/TAL1 interrupting locus; SIL; STIL; STIL_HUMAN; TAL 1 interrupting locus protein; TAL-1-interrupting locus protein.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  細胞生物  免疫學  神經生物學  信號轉導  干細胞  細胞周期蛋白  細胞分化  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Cow, Rabbit, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 143kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human STIL
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
產品介紹 background:
TAL1 disruption at 1p32, a common rearrangement in the T-cell acute lymphoblastic leukemia, usually results in the formation of a SCL interrupting locus (SIL)-TAL1 fusion product. SIL is an immediate early gene whose expression is associated with cell proliferation. The Sil protein exhibits ubiquitous expression in hematopoietic cell lines and tissues. However, Sil protein levels remain tightly regulated during the cell cycle, achieving peak levels in mitosis and diminishing on transition to G1 phase. Overexpression of Sil in primary adenocarcinomas predicts metastatic spread, especially in lung tumors with increased mitotic activity.

Function:
Immediate-early gene. Plays an important role in embryonic development as well as in cellular growth and proliferation; its long-term silencing affects cell survival and cell cycle distribution as well as decreases CDK1 activity correlated with reduced phosphorylation of CDK1. Plays a role as a positive regulator of the sonic hedgehog pathway, acting downstream of PTCH1.

Subunit:
Interacts with PIN1 via its WW domain. This interaction is dependent on STIL mitotic phosphorylation (By similarity).

Subcellular Location:
Cytoplasm, cytosol.

Tissue Specificity:
Expressed in all hematopoietic tissues and cell lines. Highly expressed in a variety of tumors characterized by increased mitotic activity with highest expression in lung cancer.

Post-translational modifications:
Phosphorylated following the activation of the mitotic checkpoint.

DISEASE:
Note=A chromosomal aberration involving STIL may be a cause of some T-cell acute lymphoblastic leukemias (T-ALL). A deletion at 1p32 between STIL and TAL1 genes leads to STIL/TAL1 fusion mRNA with STIL exon 1 slicing to TAL1 exon 3. As both STIL exon 1 and TAL1 exon 3 are 5'-untranslated exons, STIL/TAL1 fusion mRNA predicts a full length TAL1 protein under the control of the STIL promoter, leading to inappropriate TAL1 expression. In childhood T-cell malignancies (T-ALL), a type of defect such as STIL/TAL1 fusion is associated with a good prognosis. In cultured lymphocytes from healthy adults, STIL/TAL1 fusion mRNA may be detected after 7 days of culture.
Defects in STIL are the cause of microcephaly primary type 7 (MCPH7) [MIM:612703]. Microcephaly is defined as a head circumference more than 3 standard deviations below the age-related mean. Brain weight is markedly reduced and the cerebral cortex is disproportionately small. Despite this marked reduction in size, the gyral pattern is relatively well preserved, with no major abnormality in cortical architecture. Primary microcephaly is further defined by the absence of other syndromic features or significant neurological deficits.

Database links:

Entrez Gene: 6491 Human

Entrez Gene: 20460 Mouse

Entrez Gene: 313506 Rat

Omim: 181590 Human

SwissProt: Q15468 Human

SwissProt: Q60988 Mouse

Unigene: 525198 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.kastlife.cn 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
主站蜘蛛池模板: 人妻aⅴ中文字幕无码 | 色五月激情五月 | 国内免费视频成人精品 | 久艹精品| 亚洲综合在线一区 | 成年人黄色在线观看 | 一区二区三区波多野结衣在线观看 | 中文字幕无码日本欧美大片 | 噜噜爽av99| 中文精品一区二区三区四区 | 国产亚洲欧美日韩精品 | 国产乱AⅤ一区二区三区 | 精品一区二区三区视频日产 | 成年人在线免费看的惊悚动作片 | 在线免费毛片视频 | 久久一线| 人妻无码中文字幕永久有效视频 | 久久久久国产亚洲日本 | 97人人模人人爽人人少妇 | 亚洲一区二区三区国产精品 | 午夜a级毛片免费观看 | 丁香五月婷婷中文 | 欧美黄色一级 | 国产成人综合亚洲A片激情文学 | 国产精品不卡一区 | 日本免费不卡一区二区 | 1769在线视频 | 午夜精品一区二区三区三上悠亚 | Jαpαn丰满人妻HDXXXX | 性欧美freexxxx | 久久久久久久久无码精品亚洲日韩 | 国产一区二区三区不卡在线看 | 一本到不卡免费一区二区 | 日韩大片在线观看 | 色综合久久综合网 | 蜜桃av在线 | 男人扒开女人内裤强吻桶进去 | 新超碰97 | 亚卅在线有码无码免费 | 永久免费av无码国产网站 | 亚洲乱码一二三四区 |