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RabbitAnti-Properdin Rabbit pAb  antibody (bs-8306R)
~~~促销,代码KXJ230206~~~
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说明书: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价
产品编号 bs-8306R
英文名称 Properdin Rabbit pAb
中文名称 P因子/备解素抗体
别    名 BFD; PFC; PFD; PROPERDIN; BCFG; PROP_HUMAN; CFP; Complement factor P; PROP_MOUSE;   
Specific References  (2)     |     bs-8306R has been referenced in 2 publications.
111 [IF=2.96] Chen C et al. Alternative complement pathway is activated in the brains of scrapie‑infected rodents. Med Microbiol Immunol. 2019 Nov 12.  IHC-P&IHF ;  Mouse&Chinese golden hamsters.  222
111 [IF=2.81] Nashine et al. Differential Expression of Complement Markers in Normal and AMD Transmitochondrial Cybrids. (2016) PLoS.On. 11:e0159828  WB ;  Human.  222
研究领域 细胞生物  免疫学  
抗体来源 Rabbit
克隆类型 Polyclonal
克 隆 号
交叉反应 (predicted: Human, Mouse, Rat, Rabbit, )
产品应用 ELISA=1:5000-10000 IHC-P=1:100-500 (石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 48 kDa
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 Properdin: 401-469/469 
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 A positive regulator of the alternate pathway of complement. It binds to and stabilizes the C3- and C5-convertase enzyme complexes.
Involvement in disease:Defects in CFP are the cause of properdin deficiency (PFD). PFD results in higher susceptibility to bacterial infections; especially to meningococcal infections. Three phenotypes have been reported: complete deficiency (type I), incomplete deficiency (type II), and dysfunction of properdin (type III).

Function:
A positive regulator of the alternate pathway of complement. It binds to and stabilizes the C3- and C5-convertase enzyme complexes.

Subcellular Location:
Secreted

DISEASE:
Defects in CFP are the cause of properdin deficiency (PFD) [MIM:312060]. PFD results in higher susceptibility to bacterial infections; especially to meningococcal infections. Three phenotypes have been reported: complete deficiency (type I), incomplete deficiency (type II), and dysfunction of properdin (type III).

Similarity:
Contains 6 TSP type-1 domains.

SWISS:
P27918

Gene ID:
5199

Database links:

Entrez Gene: 5199 Human

Entrez Gene: 18636 Mouse

Entrez Gene: 299314 Rat

Omim: 300383 Human

SwissProt: P27918 Human

SwissProt: P11680 Mouse

Unigene: 53155 Human

Unigene: 3064 Mouse

Unigene: 204119 Rat



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