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Anti human cd29

Manufactured by BD
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Sourced in United States

Anti-human CD29 is a laboratory reagent used for the identification and characterization of cells expressing the CD29 (Integrin beta-1) antigen. CD29 is a cell surface glycoprotein involved in cell-cell and cell-matrix interactions. This product can be used in flow cytometry, immunohistochemistry, and other applications to detect the presence of CD29-positive cells.

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Lab products found in correlation

Anti human cd45, by BD (1 mentions) Anti human cd90, by BD (1 mentions) Anti human cd73, by BD (1 mentions)

Close spelling variants of this product

PE mouse anti-human CD29 APC Mouse Anti-Human CD29 APC anti-human CD29 Mouse anti-human CD29 (integrin β1)-PE PE-labeled mouse anti-human CD29 Phycoerythrin-conjugated (PE) mouse anti-human CD29 FITC-conjugated anti-human CD29 Anti-human CD29-PE Purified Rat Anti-Human CD29 PE-Cy5 mouse anti-human CD29 antibody

2 protocols using anti human cd29

1

Characterization of LPC Cell Antigens

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The specific cell surface antigens of LPCs were characterized by flow cytometry. The cells were incubated with fluorescence-conjugated antibodies at the recommended concentration for 30 min in ice. All the antibodies were obtained from BD biosciences, including anti-human CD29, CD44, CD73, CD90, CD34, CD31, CD45, anti-mouse CD44, CD31, CD34. Data analysis was performed with FlowJo software (FlowJo, Ashland, OR).
Zhang W., Zheng C., Yu T., Zhang H., Huang J., Chen L., Tong P, & Zhen G. (2022). The therapeutic effect of adipose-derived lipoaspirate cells in femoral head necrosis by improving angiogenesis. Frontiers in Cell and Developmental Biology, 10, 1014789.
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2

Characterization of hAMSC and hAEC Surface Antigens

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hAMSC and hAEC specific surface antigens were stained with PE-conjugated antibodies of anti-human-CD-105, anti-human-CD-29, anti-human-CD-44, anti-human-CD-73, anti-human-CD-90, anti-human-CD-34, anti-human-CD-45, anti-human-EpCam, or anti-human-CD-166 (BD, USA) or their corresponding isotype control. The stained cells were then analyzed respectively by fluorescence-activated cell sorting (FACS). The detailed instruction is the same as the FACS analysis already described. Differentiation ability of hAMSCs was tested using hAMSC differentiation kits for culture (Thermo, USA).
Ding C., Li H., Wang Y., Wang F., Wu H., Chen R., Lv J., Wang W, & Huang B. (2017). Different therapeutic effects of cells derived from human amniotic membrane on premature ovarian aging depend on distinct cellular biological characteristics. Stem Cell Research & Therapy, 8, 173.
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