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白介素1受體Ⅰ(IL1R1)多克隆抗體(生物素標(biāo)記)

Biotin-Linked Polyclonal Antibody to Interleukin 1 Receptor Type I (IL1R1)

CD121a; CD121-A; IL1-R1; IL1R; IL1RA; P80; CD121 Antigen-Like Family Member A; Interleukin-1 Receptor Alpha

  • 白介素1受體Ⅰ(IL1R1)多克隆抗體(生物素標(biāo)記) 產(chǎn)品包裝(模擬)
  • 白介素1受體Ⅰ(IL1R1)多克隆抗體(生物素標(biāo)記) 產(chǎn)品包裝(模擬)
  • 白介素1受體Ⅰ(IL1R1)多克隆抗體(生物素標(biāo)記) Western Blot; Sample: Raji cell lysate
    Primary Ab: 0.2μg/ml Biotin-Linked Polyclonal Antibody to Interleukin 1 Receptor Type I (IL1R1)
    Second Ab: 0.2μg/ml HRP-Labeled Streptavidin (Catalog: IS089)
  • Certificate 通過(guò)ISO 9001、ISO 13485質(zhì)量體系認(rèn)證

特異性

該抗體是針對(duì)IL1R1的兔多克隆抗體。在免疫組織化學(xué)染色和免疫印跡實(shí)驗(yàn)中能識(shí)別IL1R1。

用法

免疫印跡:0.2-2μg/mL;1:250-2500
免疫組織化學(xué):5-20μg/mL;1:25-100
免疫細(xì)胞化學(xué):5-20μg/mL;1:25-100
最佳稀釋倍數(shù)最終由用戶(hù)決定。

儲(chǔ)存

經(jīng)常使用則4°C保存。-20°C保存不超過(guò)兩年。避免反復(fù)凍融。

穩(wěn)定性

熱穩(wěn)定性以損失率顯示。損失率是由加速降解試驗(yàn)決定,具體方法如下:在37°C孵育48小時(shí),沒(méi)有顯著的降解或者沉淀產(chǎn)生。保質(zhì)期內(nèi),在適當(dāng)?shù)臈l件下存儲(chǔ),損失率低于5%。

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參考文獻(xiàn)

雜志 參考文獻(xiàn)
Clinical & Experimental Immunology In vivo extravasation induces expression of IL-1R1 in human neutrophils [Wiley: source]
PLos One The Gene Expression Analysis of Blood Reveals S100A11 and AQP9 as Potential Biomarkers of Infective Endocarditis [Plosone: 0031490]
Journal of Clinical Apheresis Kinetics of the soluble IL-1 receptor type I during treatment with an LCAP filter in patients with inflammatory bowel disease [PubMed: 22267087]
PLoS ONE A Combinatorial Relative Mass Value Evaluation of Endogenous Bioactive Proteins in Three-Dimensional Cultured Nucleus Pulposus Cells of Herniated Intervertebral Discs: Identification of Potential Target Proteins for Gene Therapeutic Approaches [Plosone: Source]
中國(guó)當(dāng)代兒科雜志 IL1R1 基因多態(tài)性與兒童哮喘的相關(guān)性 [article:13877]
STEM CELLS AND DEVELOPMENT IL-1α regulates osteogenesis and osteoclastic activity of dental follicle cells via JNK and p38 MAPK pathways [Pubmed: 33107399]
Journal of Integrative Medicine Salvadora persica extract attenuates cyclophosphamide-induced hepatorenal damage by modulating oxidative stress, inflammation and apoptosis in rats [Pubmed:35643766]
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