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
  
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
无码人妻精品一区二区二秋霞影院 ,久久国产乱子伦精品一区二区小说
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-GDF1/PE-Cy7 Conjugated antibody (bs-1794R-PE-Cy7)
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-1794R-PE-Cy7
英文名稱 Rabbit Anti-GDF1/PE-Cy7 Conjugated antibody
中文名稱 PE-Cy7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(zhuǎn)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(zhuǎn)移生長因子–β(TGF-β)家族成員。
版權(quán)所有 2004-2026 m.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
EEUSS鲁丝片直达入口音响 | 高清无码少妇一区二区 | 九色视频这里只有精品 | 全黄做爰100分钟视频 | 欧美激情一区二区三区成人小说报 | 18黄色视频在线观看 | 中文字幕人妻一区二区三区视频 | 国产人妻人伦精品九色 | 国产精品成人一区二区网站软件 | 日韩精品免费无码视频 | www.91.xhs.小黄书成人网站 | 国产www高潮呻吟在线下载 | 国产真人做爰视频免费 | 欧美国产一区二区三区 | 青青草无码成人AV片 | 国产精品21一区二区 | 精品无码又粗又大又长小说 | 变态小说之国产激情网 | 亚洲成人视频在线观看 | 中文字幕av在线观看 | 美女高潮久久久久久久 | 国产精品福利一区二区三区四季 | 亚洲天堂激情动漫视频导航 | 美女裸体插振白浆糊涂 | 国产又大又粗又黄视频 | 久久澡狠l澡欧美老妇 | 内射中出日韩无国产剧情 | 欧美理伦一二三免费看 | 91在线精品无码秘 入口 | 亚洲AV日韩精品国产成人网站 | 国产精品激烈高潮白浆 | 蜜桃aⅴ色欲A片无码精品接吻 | 国产丨熟女丨国产熟女视频 | 欧美性爱xxxx | 无码人妻丰满熟妇区毛片老年人 | 国产一级a毛一级a看… | 性感美女在线观看网站 | 国产寡妇高潮一级A片 | 成人爽a毛片一区二区免费 国产高清无码一区二区三区 | 成人无码区免费A片视频野外 | 90岁老太婆一级A片 日韩成人AV一区二区 |