Cell Reactant:
Ab N1G9
Syringe Reactant:
BDBM13
Meas. Tech.:
ITC
Entry Date.:
12/04/00
ΔG°:
-9.85±0.1 (kcal/mole)
pH:
8±n/a
Log10Kb:
4.6
Temperature:
298.65±n/a (K)
ΔH° :
-11.25±n/a (kJ/mole)
ΔHobs :
-11.25±n/a (kJ/mole)
Corrected for ΔHioniz:
not known
ΔCp :
-0.31±0.03 (kJ/mole)
ΔS° :
-0±0 (kJ/mole-K)
Citation
 Torigoe, HNakayama, TImazato, MShimada, IArata, YSarai, A The affinity maturation of anti-4-hydroxy-3-nitrophenylacetyl mouse monoclonal antibody. A calorimetric study of the antigen-antibody interaction. J Biol Chem 270:22218-22 (1995) [PubMed]  Article
Cell React
Source:
Purified from C57BL/6 mice hybridoma cell lines
Name:
Ab N1G9
Synonyms:
3B62 | N1G9
Type:
Antibody
Mol. Mass.:
47156.21
Organism:
Mus musculus (mouse)
Description:
Anti-4-hydroxy-3-nitrophenylacetyl mouse monoclonal antibody
Residue:
437
Sequence:
QVQLQQPGAELVKPGASVKLSCKASGYTFTSYWMHWVKQRPGRGLEWIGRIDPNSGGTKYNEKFKSKATLTVDKPSSTAYMQLSSLTSEDSAVYYCARYDYYGSSYFDYWGQGTTLTVSSAKTTPPSVYPLAPGSAAQTNSMVTLGCLVKGYFPEPVTVTWNSGSLSSGVHTFPAVLQSDLYTLSSSVTVPSSPWPSETVTCNVAHPASSTKVDKKIVPRDCQAVVTQESALTTSPGETVTLTCRSSTGAVTTSNYANWVQEKPDHLFTGLIGGTNNRAPGVPARFSGSLIGDKAALTITGAQTEDEAIYFCALWYSNHWVFGGGTKLTVLGQPKSSPSVTLFPPSSEELETNKATLVCTITDFYPGVVTVDWKVDGTPVTQGMETTQPSKQSNNKYMASSYLTLTARAWERHSSYSCQVTHEGHTVEKSLSRADCS
  
Syringe React
Prep. Method:
Synthesized from 4-hydroxy-3-nitrophenylacetic acid and -amino-n-caproic acid
Name:
BDBM13
Synonyms:
4-hydroxy-3-nitrophenylacetyl (NP) caproic | 6-[1-(4-hydroxy-3-nitrophenyl)acetamido]hexanoic acid
Type:
Small organic molecule
Emp. Form.:
C14H18N2O6
Mol. Mass.:
310.3025
SMILES:
OC(=O)CCCCCNC(=O)Cc1ccc(O)c(c1)[N+]([O-])=O
Structure:
Search PDB for entries with ligand similarity: