Recombinant Vibrio parahaemolyticus serotype O3:K6 Outer membrane protein ompK(ompK) CSB-EP349512VFE
Specifications
| 20ug / 100ug / 1mg price = 100ug |
Alternative Name(s):
ompK; OMPK_VIBPA; Outer membrane protein ompK
Species: (Organism)
Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633)
Gene Names:
ompK
Tag info:
N-terminal 6xHis-SUMO-tagged
Target Protein AA Sequence:
ADYSDGDIHKNDYKWMQFNLMGAFDELPGESSHDYLEMEFGGRSGIFDLYGYVDVFNLASDKGSDKVGDPKIFMKFAPRMSIDGLTGKDLSFGPVQELYVATLFEWDGTDYKTNPFSVNNQKVGIGSDVMVPWFGKVGVNLYGTYQGNQKDWNGFQISTNWFKPFYFFENGSFISYQGYIDYQFGMKEKYSSASNGGAMFNGIYWHSDRFAVGYGLKGYKDVYGIKDSDALKSTGFGHYVAVTYKF
Expression Region:
21-266aa
Subcellular Location:
Cell outer membrane
Tissue Specificity:
Protein Length:
Full Length of Mature Protein
Pathway:
Mol. Weight:
43.9 kDa
Purity:
Greater than 90% as determined by SDS-PAGE.
Form:
Liquid or Lyophilized powder
Buffer:
If the delivery form is liquid, the default storage buffer is Tris/PBS-based buffer, 5%-50% glycerol. If the delivery form is lyophilized powder, the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, pH 8.0.
Research Areas:
Others
Function:
Serves as receptor for a broad-host-range vibriophage, KVP40.
Involvement in disease:
Relevance:
Serves as receptor for a broad-host-range vibriophage, KVP40.
Reconstitution:
We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
Protein Families:
Nucleoside-specific channel-forming outer membrane porin (Tsx) (TC 1.B.10) family
Reference:
"Genome sequence of Vibrio parahaemolyticus: a pathogenic mechanism distinct from that of V. cholerae."Makino K., Oshima K., Kurokawa K., Yokoyama K., Uda T., Tagomori K., Iijima Y., Najima M., Nakano M., Yamashita A., Kubota Y., Kimura S., Yasunaga T., Honda T., Shinagawa H., Hattori M., Iida T.Lancet 361:743-749(2003)
