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(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
国产suv精品一区二区6,欧美精品在线观看,少妇激情一区二区三区久久大香香
Rabbit Anti-GDF6/RBITC Conjugated antibody (bs-11843R-RBITC)
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(jià)
產(chǎn)品編號(hào) bs-11843R-RBITC
英文名稱 Rabbit Anti-GDF6/RBITC Conjugated antibody
中文名稱 羅丹明(RBITC)標(biāo)記的生長(zhǎng)分化因子6抗體
別    名 bmp 13; bmp13; bmp-13; Cartilage Derived Morphogenetic Protein 2; cdmp 2; CDMP2; gdf 6; GDF16 ; Growth differentiation factor 6; Growth/differentiation factor 6; GDF6_HUMAN.  
規(guī)格價(jià)格 100ul/2980元 購買        大包裝/詢價(jià)
說 明 書 100ul  
研究領(lǐng)域 細(xì)胞生物  神經(jīng)生物學(xué)  信號(hào)轉(zhuǎn)導(dǎo)  生長(zhǎng)因子和激素  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Dog, Cow, Horse, Rabbit, )
產(chǎn)品應(yīng)用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 14kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human GDF6
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:
Growth/differentiation factors (GDFs) are members of the TGF superfamily (1,2). Members of the TGF superfamily are involved in embryonic development and adult tissue homeostasis (1). GDF-1 expression is almost exclusively restricted to the central nervous system and mediates cell differentiation events during embryonic development (3). Neither GDF-3 (Vgr-2) nor GDF-9 contains the conserved cysteine residue which is found in most other TGF superfamily members. GDF-3 is detectable in bone marrow, spleen, thymus and adipose tissue, whereas GDF-9 has only been detected in ovary (4). GDF-5 (also designated CDMP-1) has been shown to induce activation of plasminogen activator, thereby inducing angiogenesis. It is predominantly expressed in long bones during fetal embryonic development and is involved in bone formation. (5). GDF-5 mutations have been identified in mice with the mutation brachypodism (bp), a mutation which affects the length and number of bones in limbs (6). GDF-6 and GDF-7 are closely related to GDF-5 (6). GDF-8 has been shown to be a negative regulator of skeletal muscle mass (1).

Function:
GDF6 (Growth/differentiation factor 6) is expressed in hypertrophic chondrocytes during embryonic development of long bones and is required for normal formation of bones and joints in the limbs, skull, and axial skeleton. It plays a key role in establishing boundaries between skeletal elements during development. The functional form of GDF6 is a disulfide-linked homodimer of two 120 amino acid polypeptide chains obtained by proteolytic processing of a biologically inactive precursor protein.

Subunit:
Homodimer; disulfide-linked

Subcellular Location:
Secreted

DISEASE:
Defects in GDF6 are the cause of Klippel-Feil syndrome type 1 (KFS1) [MIM:118100]. A skeletal disorder characterized by congenital fusion of cervical vertebrae. It is due to a failure in the normal segmentation of vertebrae during the early weeks of fetal development. The clinical triad consists of short neck, low posterior hairline, and limited neck movement. Deafness is a well-known feature of KFS and may be of sensorineural, conductive, or mixed type.
Note=A chromosomal aberration involving GDF6 has been found in a patient with Klippel-Feil syndrome (KFS). Paracentric inv(8)(q22;2q23.3).
Defects in GDF6 are the cause of microphthalmia isolated type 4 (MCOP4) [MIM:613094]. A disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues. Ocular abnormalities like opacities of the cornea and lens, scaring of the retina and choroid, cataract and other abnormalities like cataract may also be present.

Similarity:
Belongs to the TGF-beta family.

Database links:
UniProtKB/Swiss-Prot: Q6KF10.1

Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權(quán)所有 2004-2026 www.nmgps.com 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)
国产精品国产成人国产三级 | 91人妻人人做人碰人人爽九色-百度 | 国产三级三级三级三级看三级 | 精品无码人妻一区二区免费蜜桃p | A片性猛交ⅩXXX乱大交 | 欧美成人精品A片免费334p | 少妇大叫太粗太大爽一区二区 | 欧美福利老妇女操大逼 | 成熟女人毛片WWW免费版在线 | 日韩欧美国产图片小说 | 国产愉拍91九色国产愉拍 | 亚洲无码在线观看视频 | 无码人妻丰满熟妇精品区东京直播 | 91成人 在线观看喷潮 | 中文字幕亚洲一区二区三区_ | 老太性开放BBBBBB | 国产亚洲无码在线观看 | 工厂大乱婬交1一7 | 青青青的成人免费视 | 黄色电影免费在线观看 | 免费国产又硬又粗视频 | 国产高潮抽搐喷白浆午夜 | 观看成人污污免费网站入口 | 少女哔哩哔哩免费观看视频 | 真正的免费毛片网站 | 成人国产精品秘 在线鲁大男同 | 久久无码一区二区三区 | 91在线无码精品秘 传媒 | av免费在线观看免费在线观看 | 亚洲AV无码秘 蜜桃希岛爱理 | 美女操bbb又爽又猛www | 无码少妇一二三四区最新版 | 亚洲日韩AV无码精品 | 红桃视频成人A片免费看 | 国产麻豆一区二区三区 | 欧美激情一区二区三级高清视频 | 老熟女又肥又大黑BBB | 无码人妻精品一区二区蜜桃漫画 | 麻豆网站少妇aaa片 神马久久久久久17. | 亚洲午夜福利在线观看 | 嫩草影院在线观看 成人版 安徽搡BBBB槡BBBB |