91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
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
麻豆乱码国产一区二区三区,上海熟妇搡BBBB搡BBBB,国产婬片lA片www777
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-STIL/Cy5.5 Conjugated antibody (bs-9303R-Cy5.5)
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-Cy5.5
英文名稱 Rabbit Anti-STIL/Cy5.5 Conjugated antibody
中文名稱 Cy5.5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(guī)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.rvdoil.com 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(yī)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
一級黃色毛毛片成人A片 | 国产无人区一区二区三区四区 | 蜜桃视频污在线免费观看 | 韩国无码电影在线观看 | 最近最好看的2018中文字幕电视剧 | 女生喷水视频在线观看 | 国产毛毛AAAAAAA做受 | 日本理论午午夜理论片 | 国产国产乱老熟女视频网站97 | 国产AV无码片毛片一级久老师 | 亚洲AⅤ无码一区二区波多野按摩 | 免费黄色视频网站免费在线观看 | 亚洲国产精品久久久 | 欧美 免费69XX| 操老女人老91妇女老熟女 | 西西444WWW无码视频软件 | 人妻精品久久久久中文字幕69 | 成人性色生活片全黄 | 四色成人A片视频在线看 | 久久精品熟妇人妻精品 | 97精品超碰一区二区三区 | 人人干人人操人人 | 在线观看av网站 | 中文字幕AV免费观看 | 91在线无码精品秘 传媒 | 影音先锋中文字幕在线观看 | 狼友视频在线观看 | 国产喷白浆一区二区三区动漫 | 欧美日韩国产一区二区三区 | 专干老妇熟女6070频 | 亚洲小说欧美激情另类A片小说 | 少妇内射精品888视频 | 欧美15一16性处交 | 中文字幕乱码在线观看 | 黄色网址在线观看视频 | 欧美性JiZZ18性欧美 | 黄片小视频在线观看免费 | 国产家庭乱日本中文一区 | 亚洲色婷婷国产精品杨思敏 | 中文字幕高清在线观看 | 午夜成人电影在线观看 |