日日操日日操,亚洲日本午夜激情,人妻内射精品一区二区,国产一区北条麻妃

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
天天射亚洲,一级福利片在线观看,日韩精品国产精品欧美在线观看
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-HESX1/BF555 Conjugated antibody (bs-13597R-BF555)
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-13597R-BF555
英文名稱 Rabbit Anti-HESX1/BF555 Conjugated antibody
中文名稱 BF555標記的同源結構域轉錄因子HESX1抗體
別    名 HESX1_HUMAN; Homeobox expressed in ES cells 1; Homeobox protein ANF; hAnf.   
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 免疫學  神經生物學  干細胞  轉錄調節(jié)因子  細胞粘附分子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
產品應用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 21kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human HESX1
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:
The homeobox protein, HESX1, which is also known as Rathke’s pouch homeobox, HANF, homeodomain transcription factor, and anterior-restricted homeobox protein is a transcription factor that belongs to the homeodomain family of DNA binding proteins. HESX1 is initially expressed in embryonic stem cells and the primitive forebrain, and is essential for normal development of the eyes and other anterior CNS structures, such as the hypothalamus, the pituitary gland and the olfactory bulbs. The homeobox gene Hesx1 is expressed in the anterior visceral endoderm (AVE), anterior axial mesendoderm (AME), and anterior neural ectoderm (ANE) during early embryogenesis. Mutations in the Hesx1 gene are associated with disorders that are comparable with septo-optic dysplasia (SOD). These disorders are characterized by hypoplasia of the optic nerve, various types of forebrain defects and pituitary hormone deficiencies, including hypothyroidism. Hesx1 also acts as a transcriptional repressor of reporter gene constructs in tissue culture assays.

Function:
Homeobox protein expressed in embryonic stem cells and targetd by Sox2, Oct4 and Nanog. Required for the normal development of the forebrain, eyes and other anterior structures such as the olfactory placodes and pituitary gland. Possible transcriptional repressor.

Subunit:
Can form heterodimers with PROP1 in binding to DNA. Interacts with TLE1.

Subcellular Location:
Nuclear

DISEASE:
Septooptic dysplasia (SOD) [MIM:182230]: A clinically heterogeneous disorder defined by any combination of optic nerve hypoplasia, pituitary gland hypoplasia with panhypopopituitarism, and midline abnormalities of the brain, including absence of the corpus callosum and septum pellucidum. Note=The disease is caused by mutations affecting the gene represented in this entry.
Growth hormone deficiency with pituitary anomalies (GHDPA) [MIM:182230]: A disease characterized by low or absent growth hormone levels, in the presence of a hypoplastic anterior pituitary lobe and ectopic or absent posterior pituitary lobe. Note=The disease is caused by mutations affecting the gene represented in this entry.
Pituitary hormone deficiency, combined, 5 (CPHD5) [MIM:182230]: Combined pituitary hormone deficiency is defined as the impaired production of growth hormone and one or more of the other five anterior pituitary hormones. CPHD5 is characterized by complete or partial deficiencies of growth hormone, thyroid-stimulating hormone, luteinizing hormone, follicle stimulating hormone and adrenocorticotropic hormone. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the ANF homeobox family.
Contains 1 homeobox DNA-binding domain.

Database links:

Entrez Gene: 8820 Human

Omim: 601802 Human

SwissProt: Q52LC5 Human

SwissProt: Q9UBX0 Human

Unigene: 171980 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 m.bklrv.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(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
九九久久区| 成人人妻视频| 国产青青草av一区二区三区四区| 久久婷婷五月综合色丁香| 综合电影一区二区三区| 欧美 日韩 亚洲 二区| 五月婷婷丁香网| 国产精品,欧美…日韩…| AV一区二区三区美国| 日韩爽爽在线观看| 五月黄色激情| 欧美熟女三级| 欧美涩情色婷婷一区二| 亚洲丰满熟女一区二区v| 亚洲日韩国产剧情一区二区| 农村妇女一区二区三区无码视频播放| 欧美一区日韩一区亚洲一区 | 无码七区6 15| 国产电影无码AV不| 久久久性生活免费视频| 在线观看亚洲av每日更新| 三级另类区| 亚洲台湾在线中文网| 91国产日韩| 噜噜噜色| 插菊综合网在线观看中文字幕亚洲| 一区二区到访日韩黄片| 大香蕉伊人丝袜| 日本精品少妇一二区| 男人94AV天堂| 久久久久伊人婷婷| 日本中文字幕在线看| 麻豆 在线观看视频| 美女国产视频网站| 哪里有日韩黄片| 人妻视频二区| 亚洲五月天无码| 日欧AV| 少妇福利12在线观看| 最新亚洲无码欧美| 精品人妻在线影院|