亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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  人才招聘  關于我們  聯系我們
国产成人精品a视频一区,无码人妻精品一二三区免费,免费永久国产在线视频
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Shh/PE Conjugated antibody (bs-1544R-PE)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-1544R-PE
英文名稱1 Rabbit Anti-Shh/PE Conjugated antibody
中文名稱 PE標記的Shh信號轉導通路膜蛋白受體抗體
別    名 Sonic hedgehog; Vhh-1; Sonic hedgehog protein; SHH; HHG 1; HHG1; HLP 3; HLP3; Holoprosencephaly 3; HPE 3; HPE3; MCOPCB5; SMMC I; SMMCI; Sonic Hedgehog (Drosophila) homolog; sonic hedgehog homolog (Drosophila); Sonic hedgehog homolog; Sonic hedgehog protein; TPT; TPTPS; Sonic hedgehog protein N-product; SHH_HUMAN.  
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  發育生物學  信號轉導  細胞膜受體  糖蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse,  (predicted: Human, Rat, Chicken, Cow, Horse, 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 19/47kDa
細胞定位 細胞膜 
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Shh
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:
SHH binds to the patched (PTC) receptor, which functions in association with smoothened (SMO), to activate the transcription of target genes. In the absence of SHH, PTC represses the constitutive signaling activity of SMO. Also regulates another target, the gli oncogene. Intercellular signal essential for a variety of patterning events during development: signal produced by the notochord that induces ventral cell fate in the neural tube and somites, and the polarizing signal for patterning of the anterior-posterior axis of the developing limb bud. Displays both floor plate- and motor neuron-inducing activity. The threshold concentration of N-product required for motor neuron induction is 5-fold lower than that required for floor plate induction (By similarity).

Function:
Binds to the patched (PTC) receptor, which functions in association with smoothened (SMO), to activate the transcription of target genes. In the absence of SHH, PTC represses the constitutive signaling activity of SMO. Also regulates another target, the gli oncogene. Intercellular signal essential for a variety of patterning events during development: signal produced by the notochord that induces ventral cell fate in the neural tube and somites, and the polarizing signal for patterning of the anterior-posterior axis of the developing limb bud. Displays both floor plate- and motor neuron-inducing activity. The threshold concentration of N-product required for motor neuron induction is 5-fold lower than that required for floor plate induction (By similarity).

Subunit:
Interacts with HHATL/GUP1 which negatively regulates HHAT-mediated palmitoylation of the SHH N-terminus. N-product is active as a multimer.

Subcellular Location:
Sonic hedgehog protein C-product: Secreted, extracellular space. Note=The C-terminal peptide diffuses from the cell. Sonic hedgehog protein N-product: Cell membrane; Lipid-anchor. Note=The N-product either remains associated with lipid rafts at the cell surface, or forms freely diffusible active multimers with its hydrophobic lipid-modified N- and C-termini buried inside.

Tissue Specificity:
Expressed in fetal intestine, liver, lung, and kidney. Not expressed in adult tissues.

Post-translational modifications:
The C-terminal domain displays an autoproteolysis activity and a cholesterol transferase activity. Both activities result in the cleavage of the full-length protein and covalent attachment of a cholesterol moiety to the C-terminal of the newly generated N-terminal fragment (N-product). The N-product is the active species in both local and long-range signaling, whereas the C-product has no signaling activity.
Cholesterylation is required for N-product targeting to lipid rafts and multimerization (By similarity).
N-palmitoylation of Cys-24 by HHAT is required for N-product multimerization and full activity (By similarity).

DISEASE:
Defects in SHH are the cause of microphthalmia isolated with coloboma type 5 (MCOPCB5) [MIM:611638]. Microphthalmia is a clinically heterogeneous disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues. Ocular abnormalities like opacities of the cornea and lens, scaring of the retina and choroid, cataract and other abnormalities like cataract may also be present. Ocular colobomas are a set of malformations resulting from abnormal morphogenesis of the optic cup and stalk, and the fusion of the fetal fissure (optic fissure).
Defects in SHH are the cause of holoprosencephaly type 3 (HPE3) [MIM:142945]. Holoprosencephaly (HPE) [MIM:236100] is the most common structural anomaly of the brain, in which the developing forebrain fails to correctly separate into right and left hemispheres. Holoprosencephaly is genetically heterogeneous and associated with several distinct facies and phenotypic variability. The majority of HPE3 cases are apparently sporadic, although clear examples of autosomal dominant inheritance have been described. Interestingly, up to 30% of obligate carriers of HPE3 gene in autosomal dominant pedigrees are clinically unaffected.
Defects in SHH are a cause of solitary median maxillary central incisor (SMMCI) [MIM:147250]. SMMCI is a rare dental anomaly characterized by the congenital absence of one maxillary central incisor.
Defects in SHH are the cause of triphalangeal thumb-polysyndactyly syndrome (TPTPS) [MIM:174500]. TPTPS is an autosomal dominant syndrome characterized by a wide spectrum of pre- and post-axial abnormalities due to altered SHH expression pattern during limb development. TPTPS mutations have been mapped to the 7q36 locus in the LMBR1 gene which contains in its intron 5 a long-range cis-regulatory element of SHH expression.

Similarity:
Belongs to the hedgehog family.

Database links:

Entrez Gene: 6469 Human

Omim: 600725 Human

SwissProt: Q15465 Human

Unigene: 164537 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

Shh是Hedgehog(Hh)信號轉導通路中分泌型信號糖蛋白,也是調控胚胎組織分化發育過程中重要因素,具有高度保守性。
版權所有 2004-2026 www.www.chomd.com.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: 国产综合内射日韩久明星| 成人免费夜片在线观看视频 | 国精品无码一区二区三区在线,在线... | 自拍偷在线精品自拍偷99,日韩好精品视频你懂的 | 国产乱码一区二区三区四区AV| 中文字幕在线视频第一页制服丝袜| 新版天堂8资源在线下载安装| 精品久久久久久综合日本-国内精品久久| 成人国产精品秘?久久久按摩下载 成人国产一区二区三区精品不卡麻豆 | 国产在线精品二区迪丽热巴2022| 中文字幕熟妇久久久人妻老牛| 日韩少妇中文字幕| 成人午夜看片在线观看,欧美| 亚洲精品无码人妻无码..,亚洲精品国| 久久久无码AV精品亚洲油麻菜| 97视频热人人精品免费,第一区 吃瓜| 无码精品前田一区二区久久久久| 国产无遮挡又黄又大又爽不卡视频| 亚洲精品字幕在线观看灌肠| 精品久久久久久无码中文字幕_久久... | 亚洲色无码一区二区三区hd| 精品人妻一区二区三区四区中文字幕 | 少妇激情av一区二区三区在线 | 少妇无码AV无码专区在线观看软件| 工口污久久婷国产精品网站| 午夜成人免费视频观看下载app| 国产免费内射又粗又爽密桃视频无码 | 久久伊精品无码二区| 中文字幕日韩亚洲欲 | 亚洲变态另类av一区二区三区在线观看| 国产主播在线一区尤物| 亚洲岛国无码爱情动作片在线观看| 国产精品五区六区香蕉| 少妇人妻精品一区二区三区黄色海洋 | 亚洲一卡2卡三卡4卡无卡下载软件 | 中文字幕中文字幕在线观看伊人| 巨茎CgGay猛男1069| 一级毛片免费不卡直播观看性色所有全部爆乳粗大 | 国产成人精品无码一区二区无码av | 国产成人无码在线精品观看| 松下纱荣子一区二区三区蜜乳中文字幕|