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(hào)           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
亚洲天堂在线观看视频,国产亲子伦XXXXX熟妇91
Rabbit Anti-GDF1/PE Conjugated antibody (bs-1794R-PE)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@bioss.com.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說(shuō) 明 書(shū): 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-1794R-PE
英文名稱 Rabbit Anti-GDF1/PE Conjugated antibody
中文名稱 PE標(biāo)記的生長(zhǎng)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(jià)格 100ul/2980元 購(gòu)買(mǎi)        大包裝/詢價(jià)
說(shuō) 明 書(shū) 100ul  
研究領(lǐng)域 心血管  神經(jīng)生物學(xué)  信號(hào)轉(zhuǎn)導(dǎo)  干細(xì)胞  生長(zhǎng)因子和激素  細(xì)胞分化  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Guinea Pig, )
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 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(chǔ) 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(zhuǎn)移生長(zhǎng)因子–β(TGF-β)家族成員。
版權(quán)所有 2004-2026 rvdoil.com 北京博奧森生物技術(shù)有限公司
通過(guò)國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書(shū)編號(hào): 00124Q34771R2M/1100
通過(guò)國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書(shū)編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
国产三级兔费视频在线观 | 中文字幕人妻丝袜成熟 | 国产成人精品午夜A片蜜 | 中文字幕日韩欧美一区二区三区 | 波多野结衣成人电影 | 91 国产丝袜在线播放竹菊 | 97人妻一区二区三区免费 | 四虎成人影视8848亚洲 | 真实的国产乱XXXX在线 | 久久AV秘 一区二区三区水生 | 久久久久亚洲AV成人精品 | 17c在线观看视频国产 | 欧美人妻在线视频video | 7777色情网黄A片免费看蜜臀 | 国产伦精品一区二区三区男技 | 国产精品一区二区五区 | 国模无码一区二区三区视频 | 中文字幕乱近親相姦视频中出恩施 | 日韩欧美国产图片小说 | 国内精品人妻无码久久久影院蜜桃 | 人妻少妇91果冻传媒麻豆 | 亚洲国产精品无码久久久久久久久 | 色欲AV性色av浪潮AV壹牛网 | 免费黄色成人网站在线看 | 国产午夜三级一区二区三 | 91中文字幕人妻在线 | 特级西西人体444WWw高清大胆 | 久久久久久久女国乱 | 天天操天天干天天日 | 一夲无码人妻一区二区 | 中文毛片无遮挡高清免费下载 | 9A蜜桃久久久久久免费 | 亚洲AV中文无码乱人 | 久久人妻少妇嫩草av | 亚洲国产精品一区二区久久阿宾 | 鲁鲁狠狠狠7777一区二区 | 白丝女仆疯狂被 自慰爽 | 亚洲精品一区二区潘金莲 | 毛片无码高清蜜桃视频 | 91久久无码一区人妻A片蜜桃 | 精品动漫二区三区无遮挡 |