强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
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  關于我們  聯(lián)系我們
欧美日韩中文字幕,国产一区二区三区在线
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-GDF1/Cy5.5 Conjugated antibody (bs-1794R-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-1794R-Cy5.5
英文名稱 Rabbit Anti-GDF1/Cy5.5 Conjugated antibody
中文名稱 Cy5.5標記的生長分化因子1抗體
別    名 DORV; DTGA3; Embryonic growth/differentiation factor 1; GDF 1; GDF-1; GDF1; GDF1_HUMAN; Growth differentiation factor 1.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 心血管  神經(jīng)生物學  信號轉導  干細胞  生長因子和激素  細胞分化  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Guinea Pig, )
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 13kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human GDF-1
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:
This gene encodes a member of the bone morphogenetic protein (BMP) family and the TGF-beta superfamily. This group of proteins is characterized by a polybasic proteolytic processing site that is cleaved to produce a mature protein containing seven conserved cysteine residues. The members of this family are regulators of cell growth and differentiation in both embryonic and adult tissues. This protein is involved in the establishment of left-right asymmetry in early embryogenesis and in neural development in later embryogenesis. This protein is transcribed from a monocistronic mRNA early in development, and from a bicistronic mRNA in later stages that also encodes the LAG1 homolog, ceramide synthase 1 gene.

Function:
May mediate cell differentiation events during embryonic development.

Subunit:
Homodimer; disulfide-linked.

Subcellular Location:
Secreted.

Tissue Specificity:
Expressed in the brain.

DISEASE:
Conotruncal heart malformations (CTHM) [MIM:217095]: A group of congenital heart defects involving the outflow tracts. Examples include truncus arteriosus communis, double-outlet right ventricle and transposition of great arteries. Truncus arteriosus communis is characterized by a single outflow tract instead of a separate aorta and pulmonary artery. In transposition of the great arteries, the aorta arises from the right ventricle and the pulmonary artery from the left ventricle. In double outlet of the right ventricle, both the pulmonary artery and aorta arise from the right ventricle. Note=The disease is caused by mutations affecting the gene represented in this entry.
Transposition of the great arteries dextro-looped 3 (DTGA3) [MIM:613854]: A congenital heart defect consisting of complete inversion of the great vessels, so that the aorta incorrectly arises from the right ventricle and the pulmonary artery incorrectly arises from the left ventricle. This creates completely separate pulmonary and systemic circulatory systems, an arrangement that is incompatible with life. The presence or absence of associated cardiac anomalies defines the clinical presentation and surgical management of patients with transposition of the great arteries. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tetralogy of Fallot (TOF) [MIM:187500]: A congenital heart anomaly which consists of pulmonary stenosis, ventricular septal defect, dextroposition of the aorta (aorta is on the right side instead of the left) and hypertrophy of the right ventricle. In this condition, blood from both ventricles (oxygen-rich and oxygen-poor) is pumped into the body often causing cyanosis. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the TGF-beta family.

Database links:

Entrez Gene: 2657 Human

Entrez Gene: 14559 Mouse

Entrez Gene: 306351 Rat

Omim: 602880 Human

SwissProt: P27539 Human

SwissProt: P20863 Mouse

Unigene: 412355 Human

Unigene: 258280 Mouse

Unigene: 202347 Rat



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

GDF-1屬于轉移生長因子–β(TGF-β)家族成員。
版權所有 2004-2026 www.nmgps.com 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(yī)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(wǎng)安備110107000727號
国产美女裸体永久免费无遮挡 | 欧美日韩一区无码 | 精品国产乱码久久久久久蜜柚 | 精品秘 无码一区二区三 | 久久成人影视白浆潮喷视频在线观看 | 小嫩美女直喷白浆在线 | 少妇精品一品二品三品在线观看 | 亚洲A片无码秘 色多多 | 黄色视频在线下载观看 | 人人看,人人澡,人人人 | 寡妇高潮一级毛片免费看 | 国产熟妇搡BBBB搡BBBB | 亚洲熟妇色自偷自拍另类 | 狼友91精品一区二区三区 | 啊娇被躁120分钟视频 | 囯产伦精一区二区三区妓 | 国偷自产Av一区二区三区换脸 | 国产午夜影院福利区 | 福利姬Jk丝袜-91Porn | 久久人人爽人人爽人人片亚洲 | 久久久91人妻无码精品蜜桃ID | 久久午夜无码鲁丝片午夜精品 | 无码人妻精品一区二区三区蜜臀 | 欧美乱大交XXXXX潮喷 | 国产极品国模粉嫩小泬 | 西西4444WWW大胆无视频双腿 | 亚洲中文字幕一区二区 | 公妇乱片A片免费看 | 色噜噜狠狠一区二区三区Av蜜芽 | 17C视频在线观看免费 | 中文在线字幕免费观看 | 国产精品入口66mio | 人妻无码中文字幕免费视频蜜桃 | 黃色A片一级一级一级久别的草原 | 亚洲无码精品一区二区 | 天天摸天天操国语对白 | 精品人妻一区二区三区浪潮无限 | 日本在线视频亚洲国产 | 久久久久久一级毛片免费 | 成年视频免费黄网站在线观看 | 国产精品伦子伦免费视频 |