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(guān)注公眾號           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  關(guān)于我們  聯(lián)系我們
在线日’B视频,国产剧情片九九精品,好屌视频国产精品
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-HESX1/Cy7 Conjugated antibody (bs-13597R-Cy7)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-13597R-Cy7
英文名稱 Rabbit Anti-HESX1/Cy7 Conjugated antibody
中文名稱 Cy7標記的同源結(jié)構(gòu)域轉(zhuǎn)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(jīng)生物學  干細胞  轉(zhuǎn)錄調(diào)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(chǎn)品應用
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(chǎn)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(quán)所有 2004-2026 m.bklrv.cn 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)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(zhì)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(wǎng)安備110107000727號
欧美一区精品久久在线| 大鸡巴干亚洲人| 午夜一及黄色电影| 成人精品ccwecc| 欧美日本一本道视频| 激情黄色日| 黄色电影区| 夫妻生活日屄视频| 欧美图片成人小说综合网| 爆操黑丝美女国产精品一区二区| 免费不卡aV在线六区| 欧美日韩伦理在线播放| 美女被操的高潮的网站| 湖州亚洲欧美日韩电车强制痴汉精品 | 超级对对碰97| 老熟曰韩欧精品| 久久精品亚洲婷婷| 隐香淫色天天影视| 欧美神马一区二区| 亚洲日韩三级在线| 久久久久久久久久中文| 精品免费一区二区三区四区| 大香蕉超碰人人| 日本XXXXXX久久久久从| 欧美一级视频黄色片| 日韩欧美一线网站在线观看| 久久视频 国产| 一区二区日本黄色| 欧美天天色高清综合网| 一区二区av新网址| 啊啊啊啊久久人人| 欧美二区综合高清在线| 一区二区入久| 欧美一区二区三区四区的| 国产精品无码免费一区二区| 国产欧美区呦呦| 天天夜夜人人狠| 国产在线theporn| 少妇后入第一区| 亚洲 成人 在线 久久| 看05Av视频|