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Gene/CloneSpeciesStageAnatomy ItemExperimenter
col1a2xenopus vertebra 

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Experiment details for col1a2

Molecular footprinting of skeletal tissues in the catshark Scyliorhinus canicula and the clawed frog Xenopus tropicalis iden...

Molecular footprinting of skeletal tissues in the catshark Scyliorhinus canicula and the clawed frog Xenopus tropicalis identifies conserved and derived features of vertebrate calcification.

Gene Clone Species Stages Anatomy
col1a2 tropicalis NF stage 54 vertebra
col1a2 tropicalis NF stage 57 vertebra

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  Figure 5. Skeletal expression patterns the Xt-Col1a1, Xt-Col1a2, and Xt-Col2a1 during Xenopus tropicalis vertebrae development. Transverse sections of stage NF54 (A–F) and NF57 (G–L) vertebrae processed for in situ hybridizations using the Xt-Col1a1, Xt-Col1a2, and Xt-Col2a1 probes, as indicated. Black arrowheads show loose (A,B) or perichondral (D–F) cells. White arrowheads in (C,I) show Xt-Col2a1 positive epithelial non-vacuolated cells of the notochord. Arrows point at osteoblasts expressing Xt-Col1a1 (G,J), Xt-Col1a2 (H,K), or Xt-Col2a1 (I,L). In (I,L), calcified, Alizarin red-positive cartilaginous regions are marked by an asterisk and the dotted lines demarcates expression boundaries between Xt-Col2a1 positive and Xt-Col2a1negative chondrocytes. In situ hybridization signal is light to dark blue. Brown endogenous X.t. pigment cells are also visible in the vicinity of the dorsal neural arch (D–F, J–L). Scale bar in (A) represents 50 μm in (A–F); scale bar in (G) represents 50 μm in (G–L).