来一水AV@lysav|亚洲AV无码片VR一区二区三区 |国产亚洲精久久久久久无码|视色4se成人午夜精品久久

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(wù)
  
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  人才招聘  關(guān)于我們  聯(lián)系我們
五月色天六月色天情网 |久久AV高潮AV无码AV喷吹|看黄子片免费网站
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-Patched/Gold Conjugated antibody (bs-1614R-Gold)
訂購熱線:400-901-9800
訂購郵箱:sales@73327.net
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@73327.net
說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-1614R-Gold
英文名稱1 Rabbit Anti-Patched/Gold Conjugated antibody
中文名稱 膠體金標記的Patched/PTCH抗體
別    名 Protein patched homolog 1; PTCH; PTC1; A230106A15Rik; BCNS; FLJ26746; FLJ42602; Holoprosencephaly 7; HPE7; mes; NBCCS; OTTHUMP00000021709; OTTHUMP00000021710; Patched; Patched (Drosophila) homolog; Patched 1; Patched homolog (Drosophila); Patched homolog 1 (Drosophila); Patched homolog 1; Patched protein homolog 1; PTC; PTC1; PTCH; PTCH protein +12b; PTCH protein +4'; PTCH protein -10; PTCH protein; PTCH1; PTCH1 protein; PTCH11; Ptch2; ; Patched / PTCH; PTC1_HUMAN.   
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
研究領(lǐng)域 腫瘤  細胞生物  發(fā)育生物學(xué)  神經(jīng)生物學(xué)  信號轉(zhuǎn)導(dǎo)  干細胞  轉(zhuǎn)錄調(diào)節(jié)因子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human, Mouse,  (predicted: Rat, Chicken, Cow, Horse, Rabbit, )
產(chǎn)品應(yīng)用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 161kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Patched/PTCH
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產(chǎn)品介紹 background:
PTCH (Patched protein homolog 1) is a receptor for sonic hedgehog (SHH), indian hedgehog (IHH) and desert hedgehog (DHH). PTCH associates with the smoothened protein (SMO) to transduce the hedgehog's proteins signal.PTCH has a tumor suppressor function, as inactivation of this protein is probably a necessary, if not sufficient step for tumorigenesis. PTCH is expressed in the adult brain, lung, liver, heart, placenta, skeletal muscle, pancreas and kidney. It is also expressed in tumor cells but not in normal skin. During development PTCH is found in all major target tissues of sonic hedgehog, such as the ventral neural tube, somites, and tissues surrounding the zone of polarizing activity of the limb bud.
Defects in PTCH are probably the cause of basal cell nevus syndrome also known as Gorlin syndrome or Gorlin-Goltz syndrome.


Function:
Acts as a receptor for sonic hedgehog (SHH), indian hedgehog (IHH) and desert hedgehog (DHH). Associates with the smoothened protein (SMO) to transduce the hedgehog's proteins signal. Seems to have a tumor suppressor function, as inactivation of this protein is probably a necessary, if not sufficient step for tumorigenesis.

Subunit:
Interacts with SNX17. Interacts with IHH.

Subcellular Location:
Membrane.

Tissue Specificity:
In the adult, expressed in brain, lung, liver, heart, placenta, skeletal muscle, pancreas and kidney. Expressed in tumor cells but not in normal skin.

Post-translational modifications:
Glycosylation is necessary for SHH binding.

DISEASE:
Defects in PTCH1 are probably the cause of basal cell nevus syndrome (BCNS) [MIM:109400]; also known as Gorlin syndrome or Gorlin-Goltz syndrome. BCNS is an autosomal dominant disease characterized by nevoid basal cell carcinomas (NBCCS) and developmental abnormalities such as rib and craniofacial alterations, polydactyly, syndactyly, and spina bifida. In addition, the patients suffer from a multitude of tumors like basal cell carcinomas (BCC), fibromas of the ovaries and heart, cysts of the skin, jaws and mesentery, as well as medulloblastomas and meningiomas. PTCH1 is also mutated in squamous cell carcinoma (SCC). Could also be associated with large body size observed in BCNS patients.
Defects in PTCH1 are a cause of sporadic basal cell carcinoma (BCC) [MIM:605462].
Defects in PTCH1 are the cause of holoprosencephaly type 7 (HPE7) [MIM:610828]. 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.

Similarity:
Belongs to the patched family.
Contains 1 SSD (sterol-sensing) domain.

Database links:

Entrez Gene: 5727 Human

Entrez Gene: 19206 Mouse

Entrez Gene: 89830 Rat

Omim: 601309 Human

SwissProt: Q13635 Human

SwissProt: Q86XG7 Human

SwissProt: Q61115 Mouse

Unigene: 494538 Human

Unigene: 228798 Mouse

Unigene: 102312 Rat



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

Ptch蛋白是細胞表面接受Hh信號蛋白的受體,目前主要用于腫瘤方面的研究。
版權(quán)所有 2004-2026 www.73327.net 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
亚洲欧美另类国产日韩| 色综合久久久久综合体桃花网| 乌克兰少妇XXXX做受野外| 国产精品一区二区更多| 国产偷人视频| 狠狠做深爱婷婷久久综合一区| 国产zzjjzzjj视频全免费| 国产精品厕所偷窥盗摄| 99久久精品国产一区二区成人了 | 欧美人妻一区黄A片| 78色精品一区二区三区| 国产产无码乱码精品久久鸭| 无码换人妻A片爽国产片| 99久久成人国产精品| 色综合久久超碰色婷婷| 中文字幕亚洲情99在线| 欧美日韩在线一区二区_国产欧美亚洲 | 男人添女人囗交做爰视频| 一区二区三区日本欧美| 国产一二三区在线播放| 两女女百合互慰AV赤裸无遮挡| 国精品人妻无码一区二区三区牛牛 | 少妇高潮惨叫正在播放对白| 国产免费一区二区视频| 日韩精品新网在线视频| 欧美老熟妇乱子伦视频| 国产精品久久久免费99| 99久久无码一区人妻| 操大爷影院| 中国白嫩丰满人妻VIDEOS| 无码一区二区三区| 日本无人区一区二区三区在线视频| 欧美激情一区二区三区不卡| 蜜芽AⅤ色欲AV浪潮夜夜嗨| 中国亚洲视频一区二区| 91人人摸人人爽人人操| 国产在线一区二区三区激情欧美| www亚洲精品少妇裸乳一区二区| 欧美精品一区二区3区| 波多野结av衣东京热无码专区| 久久久久亚洲AV无码专区桃色|