SAB4200817
Anti- Proteus vulgaris antibody produced in rabbit
IgG fraction of antiserum
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About This Item
UNSPSC Code:
12352203
Recommended Products
biological source
rabbit
antibody form
IgG fraction of antiserum
clone
polyclonal
description
Research area: Microbiome
form
buffered aqueous solution
mol wt
~70 kDa
species reactivity
Proteus vulgaris
packaging
antibody small pack of 25 μL
concentration
~1 mg/mL
technique(s)
immunoblotting: 1:20,000-1:40,000 using Proteus vulgaris LPS.
indirect ELISA: 1:20,000-1:40,000 using dead Proteus vulgaris bacteria for coating.
shipped in
dry ice
storage temp.
−20°C
target post-translational modification
unmodified
General description
Proteus vulgaris is a Gram negative rod-shaped bacteria, belongs to the Enterobacteriaceae family. Members of the genus Proteus (Proteus spp.) which also includes Proteus mirabilis, Proteus penneri and Proteus hauseri, originally characterize by their ability to swarm on solid surfaces, are widespread in the environment and the gastrointestinal tract of human and animals and known to be an opportunistic pathogens isolated from urine, wounds and other clinical sources. The Proteus spp. bacteria, are distinguished by their reactions for indole production, salicin fermentation and aesculin hydrolysis. P. vulgaris produces indole which differentiates it from the indole-negative P. mirabilis and P. penneri. Proteus spp. bacteria may also be found in soil or water habitats where they often regarded as indicators of fecal pollution and a contamination threat for potential water or seafood poisoning.
Immunogen
Proteus vulgaris dead OX19 bacteria: ATCC strain 6380
Application
Anti-Proteus vulgaris antibody recognizes P. vulgaris whole extract and P. vulgaris LPS, the antibody also recognizes an additional ~70kDa band suspected as bacterial HSP70 (DNAK) in whole extract P. mirabilis, P. gingivalis, E.coli K-12, P.aeruginosa, S. flexneri, S. enterica and E. faecalis but it has no cross reactivity with P. mirabilis LPS. The antibody may be used in various immunochemical techniques including Immunoblotting and ELISA.
Physical form
Supplied as a solution in 0.01 M phosphate buffered saline pH 7.4, containing 15 mM sodium azide as a preservative.
Disclaimer
This product is for R&D use only, not for drug, household, or other uses.
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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The effect of p-nitrophenylglycerol on swarming and the production of some virulence factors in Proteus vulgaris
Ghaidaa M, et al.
New York Science Journal, 6, 8-14 (2013)
ANTIMICROBIAL RESISTANCE PATTERNS OF PROTEUS ISOLATES FROM CLINICAL SPECIMENS
Bahashwan, et al.
EUROPEAN SCIENTIFIC JOURNAL, 9, 188-202 (2013)
C M O'Hara et al.
International journal of systematic and evolutionary microbiology, 50 Pt 5, 1869-1875 (2000-10-18)
Strains traditionally identified as Proteus vulgaris formed three biogroups. Biogroup 1, characterized by negative reactions for indole production, salicin fermentation and aesculin hydrolysis, is now known as Proteus penneri. Biogroup 2, characterized by positive reactions for indole, salicin and aesculin
N Pal et al.
Annals of medical and health sciences research, 6(5), 267-273 (2017-05-16)
Proteus species cause a variety of community- and hospital-acquired illnesses. Synthesis of β-lactamases is the predominant mechanism for resistance to β-lactam antibiotics. Among the β-lactamases, extended spectrum β-lactamases (ESBLs) and AmpC β-lactamases are the most common. The objective of this
Dominika Drzewiecka
Microbial ecology, 72(4), 741-758 (2016-10-27)
Proteus spp. bacteria were first described in 1885 by Gustav Hauser, who had revealed their feature of intensive swarming growth. Currently, the genus is divided into Proteus mirabilis, Proteus vulgaris, Proteus penneri, Proteus hauseri, and three unnamed genomospecies 4, 5
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