来一水AV@lysav|亚洲AV无码片VR一区二区三区 |国产亚洲精久久久久久无码|视色4se成人午夜精品久久

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  人才招聘  關(guān)于我們  聯(lián)系我們
亚洲熟妇av不卡一区二区三区|亚洲熟妇av一区
Rabbit Anti-GDF1/Cy5.5 Conjugated antibody (bs-1794R-Cy5.5)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@73327.net
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@73327.net
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-1794R-Cy5.5
英文名稱1 Rabbit Anti-GDF1/Cy5.5 Conjugated antibody
中文名稱 Cy5.5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        大包裝/詢價(jià)
說 明 書 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 www.73327.net 北京博奧森生物技術(shù)有限公司
通過國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號(hào): 00124Q34771R2M/1100
通過國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
亚洲 小说 欧美 激情 另类| 成人午夜精品久久久久| 无码人妻丰满熟妇区五十路| 熟妇人妻av无码一区二区三区| ASS白嫩白嫩的少妇PICS| 久久er热免费视频综合成人网| 欧美性受XXXX黑人XYX性爽| 日本精品久久久久久久久| 久久国产精品-国产精品 | 在线看片国产日韩欧美亚洲 | 无遮挡十八禁在线视频国产| 精品国产一区二区三区AV性色 | 精产国品一二三产区区别| JIZZ中国JIZZ免费| 欧美好大好爽视频| 国产乱子伦精品中文| 人妻无码αv中文字幕久久琪琪布| 亚洲欧美日韩久久久久久| 国产产无码乱码精品久久鸭| 风流少妇又紧又爽又丰满| 国产精品高潮呻吟毛片av| 免费观看黃色A片观看| 国产精品福利久久久| 你懂的电影| 免费无码一线A片AAA片| 大乳丰满人妻中文字幕日本| 国产精品久久久久久爽爽爽床戏| 国产欧美日韩国产欧美日韩| 亚洲中文字幕有码一区二区| 内射人妻少妇无码一本一道| 老熟妇高潮一区二区三区| 夜夜爽www| a片在线观看免费| 亚洲av污精品一区二区三区| 男生被男人CAO屁股的后果| 100国产精品人妻无码| 激情综合婷婷色五月蜜桃| 国产熟女一区二区三区五月婷| 亚洲国产高清国产拍精品| 国产精品爱久久久久久久| 国产av人人夜夜澡人人爽麻豆 |