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. 1998 Jul 13;142(1):167–179. doi: 10.1083/jcb.142.1.167

Table I.

STOP and Tubulin Labeling of Microtubules in DRG Cell Axons

STOP Glu-tubulin Tyr-tubulin Δ2-tubulin
T MTs  
 m  12.8  11.0  21.4  19.3
 SEM   0.3   0.2   0.6   0.5
n 523 397 333 376
CS MTs
 m  21.4  21.3  17.0  21.9
 SEM   0.6   0.5   0.5   0.6
n 295 261 167.0 236.0
CL MTs
 m   4.2   0.7  25.8  16.7
 SEM   0.8   0.6   1.3   1.2

DRG cells were either untreated or exposed to cold temperature. Cells were further reacted either with the affinity-purified 23C STOP antibody or with one isoform specific tubulin antibody (Tyr-, Glu- or Δ2-tubulin antibody) and with secondary gold-labeled antibody. The table shows the mean numbers of gold particles observed per 500 nm of microtubule length for total (T MTs) and cold-stable (CS MTs) polymers. The corresponding mean numbers for cold-labile microtubules (CL MTs) were estimated as described under Materials and Methods. m, mean number of gold particle per 500 nm of microtubule length. SEM, standard error of the mean. n, number of microtubules examined.