Recombinant Neisseria meningitidis serogroup B Quinolinate synthase A(nadA) CSB-EP878213NGG
Specifications
| 20ug / 100ug / 1mg price = 100ug |
Alternative Name(s):
nadA; NMB0394; Quinolinate synthase A; EC 2.5.1.72
Species: (Organism)
Neisseria meningitidis serogroup B (strain MC58)
Gene Names:
nadA
Tag info:
N-terminal 6xHis-tagged
Target Protein AA Sequence:
MQTAARRSFDYDMPLIQTPTSACQIRQAWAKVADTPDRETADRLKDEIKALLKEKNAVLVAHYYVDPLIQDLALETGGCVGDSLEMARFGAEHEAGTLVVAGVRFMGESAKILCPEKTVLMPDLEAECSLDLGCPEEAFSAFCDQHPDRTVVVYANTSAAVKARADWVVTSSVALEIVSYLKSRGEKLIWGPDRHLGDYICRETGADMLLWQGSCIVHNEFKGQELAALKAEHPEAVVLVHPESPQSVIELGDVVGSTSKLLKAAVSRPEKKFIVATDLGILHEMQKQAPDKQFIAAPTAGNGGSCKSCAFCPWMAMNSLGGIKYALTSGRNEILLDRKLGEAAKLPLQRMLDFAAGLKKKDVFNGMGPA
Expression Region:
1-370aa
Subcellular Location:
Cytoplasm
Tissue Specificity:
Protein Length:
Full Length
Pathway:
Mol. Weight:
44.2 kDa
Purity:
Greater than 85% 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:
Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate.
Involvement in disease:
Relevance:
Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate.
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:
Quinolinate synthase A family, Type 1 subfamily
Reference:
"Expression of the meningococcal adhesin NadA is controlled by a transcriptional regulator of the MarR family." Schielke S., Huebner C., Spatz C., Nagele V., Ackermann N., Frosch M., Kurzai O., Schubert-Unkmeir A. Mol. Microbiol. 72:1054-1067(2009)
