99精品欧美一区二区三区综合在线,国产精品一区二区的,欧美亚洲国产日韩综合,99精品视频在线观看2

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
欧美大片免费影院在线观看,欧美日韩国产另类一区
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
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@www.eweiwc.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@www.eweiwc.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標記的膠質(zhì)細胞源性神經(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  細胞凋亡  生長因子和激素  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse, Rat,  (predicted: Human, Chicken, Dog, Pig, Cow, Horse, Rabbit, )
產(chǎn)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 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)生物學相關(guān)蛋白
版權(quán)所有 2004-2026 www.www.eweiwc.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
老熟妇高潮一区二区高清视频| 美女的粉嫩小逼视频特写| 国产一区二区三区 韩国女主播| 日本美女阴户射尿| 国产一区二区三区 韩国女主播| 中文字幕不卡一区二区免| 综合欧美日韩一区二区三区| 大鸡吧插美女嫩逼| 裸体美女被操的啊啊直叫| 欧美在线A片一区二区三区| 91秦先生全集在线观看| 国产 推油 性爱| 亚洲国产综合精品 在线 一区| 被春药女高潮抽搐喷水视频| 欧美国产日韩a欧美在线| 女同舔我下面直流水| 国产一区精品在线| 淫荡扣逼骚逼视频| 精品一区二区av天堂色偷偷| 女人被男人操到高潮视频| 日韩素人精品亚洲热一区| 胸大裸体美女视频| 公交车上被后入搞逼漫画| 中文字幕在线观视频| 97人人澡人人爽人人揉| 夫妻性生活在线免费视频| 伊人网在线免费视频| 精品国产自在久国产应用| 又大黄又硬又爽免费视频| 操大美女逼射精视频| 奇米一区二区三区视频在线观看| 大黑屌爆操日本女人| 成人高清在线播放一区二区三区| 激情亚洲人妻精品| 青青视频在线人视频在线| 欧洲美熟女乱又伦| 中文字幕国产精品一区二区三区| 2021最新热播国产一区二区| 尤物性生活午夜在线视频| 国产精品一区二区三区涩涩av| 鸡巴操美女小穴羞羞视频|