扫码关注公众号           扫码咨询技术支持           扫码咨询技术服务
  
客服热线:400-901-9800  客服QQ:4009019800  技术答疑  技术支持  质量反馈  关于我们  联系我们
产品中心-北京博奥森生物技术有限公司
首页 > 产品中心 > 一抗 > 产品信息
FGF10 Rabbit pAb (bs-1326R)  
订购热线:400-901-9800
订购邮箱:sales@bioss.com.cn
订购QQ:  400-901-9800
技术支持:techsupport@bioss.com.cn
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价

产品编号 bs-1326R
英文名称 FGF10 Rabbit pAb
中文名称 成纤维细胞生长因子10抗体
别    名 Fibroblast growth factor 10; FGF 10; FGF-10; Keratinocyte growth factor 2; KGF 2; BB213776; fd11d03; FGF10_HUMAN; wu:fd11d03; zgc:109774.  
Specific References  (4)     |     bs-1326R has been referenced in 4 publications.
[IF=2.91] Zhang Y et al. Comparative study on seasonal hair follicle cycling by analysis of the transcriptomes from cashmere and milk goats. Genomics. 2019 Feb 16. pii: S0888-7543(18)30576-7.  WB ;  Goat.  
[IF=2.173] Liu K et al. FGF10 regulates thalamocortical axon guidance in the developing thalamus. Neurosci Lett. 2020 Jan 18;716:134685.  IHF ;  chick.  
[IF=1.7] Huang, Jian, et al. "Expression of bioactive recombinant human fibroblast growth factor 10 in Carthamus tinctorius L. seeds." Protein Expression and Purification (2015).  WB ;  
[IF=1.559] Chen et al. Sonic hedgehog protein regulates fibroblast growth factor 8 expression in metanephric explant culture from BALB/c mice: Possible mechanisms associated with renal morphogenesis. (2016) Mol.Med.Re. 14:2929-36  IF(IHC-P) ;  Mouse.  
研究领域 肿瘤  心血管  免疫学  信号转导  干细胞  生长因子和激素  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human (predicted: Mouse,Rat,Rabbit,Pig,Sheep,Cow,Chicken,Dog,GuineaPig,Horse)
产品应用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 23 kDa
检测分子量
细胞定位 分泌型蛋白 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human FGF10: 101-208/208 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein exhibits mitogenic activity for keratinizing epidermal cells, but essentially no activity for fibroblasts, which is similar to the biological activity of FGF7. Studies of the mouse homolog of suggested that this gene is required for embryonic epidermal morphogenesis including brain development, lung morphogenesis, and initiation of lim bud formation. This gene is also implicated to be a primary factor in the process of wound healing. [provided by RefSeq, Jul 2008]

Function:
Plays an important role in the regulation of embryonic development, cell proliferation and cell differentiation. Required for normal branching morphogenesis. May play a role in wound healing.

Subunit:
Interacts with FGFR1 and FGFR2. Interacts with FGFBP1.

Subcellular Location:
Secreted (Potential).

DISEASE:
Defects in FGF10 are the cause of autosomal dominant aplasia of lacrimal and salivary glands (ALSG) [MIM:180920]. ALSG has variable expressivity, and affected individuals may have aplasia or hypoplasia of the lacrimal, parotid, submandibular and sublingual glands and absence of the lacrimal puncta. The disorder is characterized by irritable eyes, recurrent eye infections, epiphora (constant tearing) and xerostomia (dryness of the mouth), which increases the risk of dental erosion, dental caries, periodontal disease and oral infections. Defects in FGF10 are a cause of lacrimo-auriculo-dento-digital syndrome (LADDS) [MIM:149730]; also known as Levy-Hollister syndrome. LADDS is a form of ectodermal dysplasia, a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. LADDS is an autosomal dominant syndrome characterized by aplastic/hypoplastic lacrimal and salivary glands and ducts, cup-shaped ears, hearing loss, hypodontia and enamel hypoplasia, and distal limb segments anomalies. In addition to these cardinal features, facial dysmorphism, malformations of the kidney and respiratory system and abnormal genitalia have been reported. Craniosynostosis and severe syndactyly are not observed.

Similarity:
Belongs to the heparin-binding growth factors family.

SWISS:
O15520

Gene ID:
2255

Database links:

Entrez Gene: 2255 Human

Entrez Gene: 14165 Mouse

Entrez Gene: 25443 Rat

Omim: 602115 Human

SwissProt: O15520 Human

SwissProt: O35565 Mouse

SwissProt: P70492 Rat

Unigene: 664499 Human

Unigene: 317323 Mouse

Unigene: 44439 Rat



FGF-10对于角质形成细胞的异常增殖和分化异常可能有着重要的调节作用。有学者认为;部分肿瘤、胚胎发育紊乱、生长发育障碍性疾病、炎症及修复异常、免疫性疾病、血液病、HIV感染等都与FGF-10有关。
产品图片
Sample: SW480 (human)cell Lysate at 40 ug Primary: Anti-FGF10(bs-1326R)at 1/300 dilution Secondary: IRDye800CW Goat Anti-RabbitIgG at 1/20000 dilution Predicted band size: 23 kD Observed band size: 17 kD
Sample:U251 (human)cell Lysate at 40 ug Primary: Anti-FGF10(bs-1326R)at 1/300 dilution Secondary: IRDye800CW Goat Anti-RabbitIgG at 1/20000 dilution Predicted band size: 23 kD Observed band size: 18 kD
版权所有 2004-2026 www.bioss.com.cn 北京博奥森生物技术有限公司
通过国际质量管理体系ISO 9001:2015 GB/T 19001-2016    证书编号: 00124Q34771R2M/1100
通过国际医疗器械-质量管理体系ISO 13485:2016 GB/T 42061-2022    证书编号: CQC24QY10047R0M/1100
京ICP备05066980号-1         京公网安备110107000727号