产品名称
溶葡球菌酶 来源于溶葡萄球菌, BioUltra, ≥97% (SDS-PAGE), Protein 40-60 % by biuret, ≥2,000 units/mg protein
biological source
bacterial (Staphylococcus sp.)
product line
BioUltra
assay
≥97% (SDS-PAGE)
form
lyophilized powder
specific activity
≥2,000 units/mg protein
mol wt
25 kDa
composition
Protein, 40-60% biuret
concentration
40—60% protein
technique(s)
cell based assay: suitable
suitability
suitable for cell lysis
antibiotic activity spectrum
Gram-positive bacteria
application(s)
diagnostic assay manufacturing
mode of action
cell wall synthesis | interferes
storage temp.
−20°C
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Biochem/physiol Actions
溶葡萄球菌素是一种分子量约为25 kDa的锌内肽酶。 由于溶葡萄球菌酶能裂解 葡萄球菌 类细胞壁肽聚糖层中的聚甘氨酸交联键,它已被发现可用于细胞裂解,并具有潜在的抗菌治疗作用。
活性最佳pH:约 7.5
活性最佳pH:约 7.5
General description
包装尺寸基于蛋白质含量
化学结构:肽
Other Notes
一个单位在 25°C 和 pH 7.5 条件下,在 6.0 ml 反应混合物中可使金黄色酿脓葡萄球菌细胞悬浮液的浊度(A620)在 10 分钟内由 0.250 降至 0.125。
Physical form
含有磷酸钾缓冲盐和氯化钠
Preparation Note
亲和纯化
signalword
Danger
hcodes
Hazard Classifications
Resp. Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
常规特殊物品
此项目有
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Nasal colonization of Staphylococcus aureus (S.aureus) is known as a significant risk factor for nosocomial infections, and clearance of its nasal colonization greatly reduces the risk. In the present study the preparation and characterizations of the chitosan-o/w cream incorporated with
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Lysostaphin (LS), a naturally occurring Staphylococcal endopeptidase, has the ability to penetrate biofilm, and has been identified as a potential antimicrobial to prevent mesh infection. The goals of this study were to determine if LS adhered to porcine mesh (PM)
A P Desbois et al.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 30(8), 1015-1021 (2011-02-12)
Drug-resistant staphylococci constitute a serious problem that urgently requires the discovery of new therapeutic agents. There has been a resurgence in interest in using lysostaphin (a specific anti-staphylococcal enzyme) as a treatment for infections caused by these important pathogens. However
Martin Bjerregård Pedersen et al.
Journal of immunology (Baltimore, Md. : 1950), 184(4), 1931-1945 (2010-01-08)
The binding of Abs to microbial surfaces followed by complement activation constitutes an important line of defense against infections. In this study, we have investigated the relationship between complement activation and the binding of human IgM Abs to surfaces with
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