SurA | SurA

405 €

AS10 798   | clonality: polyclonal  |  host: rabbit  |  reactivity: Yersinia pseudotuberculosis


20 st
Item No:
AS10 798

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product information

SurA (stationary phase survival) is a periplasmic chaperone and folding catalyst with peptidyl-prolyl cis-trans isomerase activity. It is involved in the maintenance of Gram-negative bacterial envelope integrity and the transport/assembly of a subset of OMPs.


Recombinant SurA over-expressed as a N-terminal fusion with His(x6)-tag, which was removed prior to immunization. UniProt protein accession number B1JKY1; NCBI annotated locus tag YPK_3571

Host Rabbit
Clonality Polyclonal
Purity Serum
Format Lyophilized
Quantity 100 ĩl
Reconstitution For reconstitution add 100 ĩl of sterile water.

store lyophilized/reconstituted at -20°C; once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please, remember to spin tubes briefly prior to opening them to avoid any losses that might occur from lyophilized material adhering to the cap or sides of the tubes.

Tested applications western blot (WB)
Related products

secondary antibodies

Additional information

to be added when available

application information
Recommended dilution

1 : 5000 with standard ECL (WB)

Expected | apparent MW

47.7 | 52 kDa

Confirmed reactivity

Yersinia pseudotuberculosis

Predicted reactivity

Yersinia pestis, Yersinia enterocolitica and related species

Not reactive in

no confirmed exceptions from predicted reactivity known in the moment

Additional information

In WB, lower molecular weight cross-reacting bands exist at approximately 34 kDa and 24 kDa. Neither of these interfere with SurA identification.

Selected references

to be added when available

application example

 Approximately 10 µg of total protein from Y. pseudotuberculosis    extracted with   were separated on 12 % SDS-PAGE and blotted 1h to PVDF. Blots were blocked immediately following  transfer in milk solution (10 % milk powder in TBST) for 1 h at room temperature with agitation. Blots were incubated in the primary antibody at a dilution of 1: 5 000 overnight at  4 °C with agitation. The antibody solution was decanted and the blot was washed twiced for 15 min in TBST at room temperature with agitation. Blots were incubated in secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated, from GE Healthcare) diluted to 1: 20 000 in  for 1h at room temperature with agitation. The blots were washed as above and developed for 35 min with homemade ECL  detection reagent. Exposure time was 60  seconds.


western blot using anti-SurA antibody

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