| 產(chǎn)品編號(hào) | bs-1326R |
| 英文名稱(chēng) | Rabbit Anti-FGF10 antibody |
| 中文名稱(chēng) | 成纖維細(xì)胞生長(zhǎng)因子10抗體 |
| 別 名 | Fibroblast growth factor 10; FGF 10; FGF-10; Keratinocyte growth factor 2; KGF 2; BB213776; fd11d03; FGF10_HUMAN; wu:fd11d03; zgc:109774. |
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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.
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| 研究領(lǐng)域 | 腫瘤 心血管 免疫學(xué) 信號(hào)轉(zhuǎn)導(dǎo) 干細(xì)胞 生長(zhǎng)因子和激素 |
| 抗體來(lái)源 | Rabbit |
| 克隆類(lèi)型 | Polyclonal |
| 交叉反應(yīng) | Human (predicted: Mouse,Rat,Rabbit,Pig,Sheep,Cow,Chicken,Dog,GuineaPig,Horse) |
| 產(chǎn)品應(yīng)用 | WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 理論分子量 | 23kDa |
| 細(xì)胞定位 | 分泌型蛋白 |
| 性 狀 | Liquid |
| 濃 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human FGF10: 101-208/208 |
| 亞 型 | IgG |
| 純化方法 | affinity purified by Protein A |
| 緩 沖 液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| 保存條件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 注意事項(xiàng) | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| PubMed | PubMed |
| 產(chǎn)品介紹 |
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 Omim: 602115 Human SwissProt: O15520 Human SwissProt: O35565 Mouse Unigene: 664499 Human Unigene: 317323 Mouse Unigene: 44439 Rat FGF-10對(duì)于角質(zhì)形成細(xì)胞的異常增殖和分化異常可能有著重要的調(diào)節(jié)作用。有學(xué)者認(rèn)為；部分腫瘤、胚胎發(fā)育紊亂、生長(zhǎng)發(fā)育障礙性疾病、炎癥及修復(fù)異常、免疫性疾病、血液病、HIV感染等都與FGF-10有關(guān)。 |
| 產(chǎn)品圖片 |
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
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