Rabbit Anti-COL10A1 Recombinant Antibody (C11093) (V2LY-1206-LY588)

Lv, D., Chen, D., Wang, Z., Cui, Z., Ma, J. H., Ji, S., ... & Tang, S. (2022). COL10A1 is a novel factor in the development of choroidal neovascularization. Microvascular Research, 139, 104239.

Chen, S., Wei, Y., Liu, H., Gong, Y., Zhou, Y., Yang, H., & Tang, L. (2021). Analysis of Collagen type X alpha 1 (COL10A1) expression and prognostic significance in gastric cancer based on bioinformatics. Bioengineered, 12(1), 127-137.

Wu, H., Wang, S., Li, G., Yao, Y., Wang, N., Sun, X., ... & Xu, C. (2021). Characterization of a novel COL10A1 variant associated with Schmid‐type metaphyseal chondrodysplasia and a literature review. Molecular genetics & genomic medicine, 9(5), e1668.

Yang, W., Wu, X., & Zhou, F. (2021). Collagen Type X Alpha 1 (COL10A1) Contributes to Cell Proliferation, Migration, and Invasion by Targeting Prolyl 4-Hydroxylase Beta Polypeptide (P4HB) in Breast Cancer. Medical Science Monitor: International Medical Journal of Experimental and Clinical Research, 27, e928919-1.

Aktas, S. H., Taskin-Tok, T., Al-Khafaji, K., & Akın-Balı, D. F. (2021). A detailed understanding of the COL10A1 and SOX9 genes interaction based on potentially damaging mutations in gastric cancer using computational techniques. Journal of Biomolecular Structure and Dynamics, 1-12.

Zhang, M., Chen, H., Wang, M., Bai, F., & Wu, K. (2020). Bioinformatics analysis of prognostic significance of COL10A1 in breast cancer. Bioscience Reports, 40(2).

Zhang, X., Liang, H., Liu, W., Li, X., Zhang, W., & Shang, X. (2019). A novel sequence variant in COL10A1 causing spondylometaphyseal dysplasia accompanied with coxa valga: A case report. Medicine, 98(30).

Huang, H., Li, T., Ye, G., Zhao, L., Zhang, Z., Mo, D., ... & Liu, H. (2018). High expression of COL10A1 is associated with poor prognosis in colorectal cancer. OncoTargets and therapy, 11, 1571.

Zhang, C., Liu, J., Iqbal, F., Lu, Y., Mustafa, S., Bukhari, F., ... & Xu, S. (2018). A missense point mutation in COL10A1 identified with whole-genome deep sequencing in a 7-generation Pakistan dwarf family. Heredity, 120(1), 83-89.

ul Ain, N., Makitie, O., & Naz, S. (2018). Autosomal recessive chondrodysplasia with severe short stature caused by a biallelic COL10A1 variant. Journal of Medical Genetics, 55(6), 403-407.

Please try the standard protocols which include: protocols, troubleshooting and guide.

Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme Linked Immunospot (ELISpot)
Proteogenomic
Other Protocols