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(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  關(guān)于我們  聯(lián)系我們
少妇把腿扒开让我添69式mv,,丰满少妇A级毛片,人妻纶乱A级毛片免费看初女
Rabbit Anti-GDNF/PE-Cy5.5 Conjugated antibody (bs-1024R-PE-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(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-1024R-PE-Cy5.5
英文名稱 Rabbit Anti-GDNF/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5標(biāo)記的膠質(zhì)細(xì)胞源性神經(jīng)營養(yǎng)因子抗體
別    名 glial cell line derived neurotrophic factor; Astrocyte derived trophic factor 1; Astrocyte derived trophic factor; ATF 1; ATF 2; ATF1; ATF2; Glial cell derived neurotrophic factor; Glial derived neurotrophic factor; HFB1 GDNF; GDNF_HUMAN; Atf; gdnf; Glial Cell Line Derived Neurotrophic Factor; Glial cell line-derived neurotrophic factor; Glial derived neurotrophic factor; hGDNF; HSCR3.   
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 神經(jīng)生物學(xué)  細(xì)胞凋亡  生長因子和激素  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Mouse, Rat,  (predicted: Human, Chicken, Dog, Pig, Cow, Horse, Rabbit, )
產(chǎn)品應(yīng)用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 15kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human GDNF
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:
Neurobiology. Neurotrophins. Neuroscience.
This gene encodes a highly conserved neurotrophic factor. The recombinant form of this protein was shown to promote the survival and differentiation of dopaminergic neurons in culture, and was able to prevent apoptosis of motor neurons induced by axotomy. The encoded protein is processed to a mature secreted form that exists as a homodimer. The mature form of the protein is a ligand for the product of the RET (rearranged during transfection) protooncogene. In addition to the transcript encoding GDNF, two additional alternative transcripts encoding distinct proteins, referred to as astrocyte-derived trophic factors, have also been described. Mutations in this gene may be associated with Hirschsprung disease.


Function:
Neurotrophic factor that enhances survival and morphological differentiation of dopaminergic neurons and increases their high-affinity dopamine uptake.

Subunit:
Homodimer; disulfide-linked.

Subcellular Location:
Secreted.

Tissue Specificity:
In the brain, predominantly expressed in the striatum with highest levels in the caudate and lowest in the putamen. Isoform 2 is absent from most tissues except for low levels in intestine and kidney. Highest expression of isoform 3 is found in pancreatic islets. Isoform 5 is expressed at very low levels in putamen, nucleus accumbens, prefrontal cortex, amygdala, hypothalamus and intestine. Isoform 3 is up-regulated in the middle temporal gyrus of Alzheimer disease patients while isoform 2 shows no change.

DISEASE:
Defects in GDNF may be a cause of Hirschsprung disease type 3 (HSCR3) [MIM:613711]. In association with mutations of RET gene, defects in GDNF may be involved in Hirschsprung disease. This genetic disorder of neural crest development is characterized by the absence of intramural ganglion cells in the hindgut, often resulting in intestinal obstruction.
Defects in GDNF are a cause of congenital central hypoventilation syndrome (CCHS) [MIM:209880]; also known as congenital failure of autonomic control or Ondine curse. CCHS is a rare disorder characterized by abnormal control of respiration in the absence of neuromuscular or lung disease, or an identifiable brain stem lesion. A deficiency in autonomic control of respiration results in inadequate or negligible ventilatory and arousal responses to hypercapnia and hypoxemia.

Similarity:
Belongs to the TGF-beta family. GDNF subfamily.

Database links:

Entrez Gene: 2668 Human

Entrez Gene: 14573 Mouse

Entrez Gene: 25453 Rat

Omim: 600837 Human

SwissProt: P39905 Human

SwissProt: P48540 Mouse

SwissProt: Q07731 Rat

Unigene: 248114 Human

Unigene: 4679 Mouse

Unigene: 53970 Rat



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

神經(jīng)生物學(xué)相關(guān)蛋白
版權(quán)所有 2004-2026 www.rvdoil.com 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
国精品无码一区二区三区在线秋菊 | 亚洲国产精品无码久久久久 | 午夜激情视频在线观看 | 7777色情网黄A片免费看蜜臀 | 少妇做爰特黄A片免费看9 | 奴色虐aV一区二区三区 | 成人区.com免费观看 | 高清欧美性猛交XXXX黑人猛交 | 99人妻人人揉人人澡人人 | 黄片一区二区三区四区五区六区七区 | 国产日韩成人精品一区二区 | 成人无码做爰www免费 | 国产高潮呻吟精品无码 | 舌L子伦熟妇αV无码视频 | 波多野结衣无码在线 | 亚洲精品无码乱码成人果冻传媒 | 亚州精品一区二区视频网站 | 舔逼嫩白浆小穴图片 | 无码人妻丰满熟妇BBB在线 | 国产男女扒开腿做爽爽 | 国内精品久久久久久久星 | 四川少妇丰满一级毛片 | 色欲av秘 臀av高清红桃 | 国产农村妇女一级A片免黑人 | 亚洲 欧洲 偷拍 自拍 | 日韩毛片在线观看 | 亚洲色七久久桃花精品影院 | 亚洲自拍偷拍中文无码 | 免费黄色片在线播放 | 国产人妻人伦精品熟女A玄幻 | 农村婬乱男女A片爽视频麻豆软件 | 黄色视频在线网站上免费观看不用下载 | 国产农村色情一二三区 | 日韩 欧美 在线观看 | 中文字幕日韩精品人妻 | 国产一区二区三区在线 | 做爰高潮A片AAA视频 | 少妇一级婬片50分钟 | 国产又粗又猛又黄又爽 | 河南少妇搡BBBB搡BBBB | 国产级AA大片免费久久久久久 |