Show Order Info
Pack Size:1mg
Application:ELISA, IF, IHC, ICC, WB
Data & Images


Goat Anti-rabbit IgG secondary antibody, Unconjugated contains affinity-purified antibodies with well-characterized specificity for Rabbit IgG (whole molecule) and are useful in the detection of their specified targets through IHC-P,IHC-F,ICC,IF,WB,ELISA.


Product Name Goat Anti-Rabbit IgG Secondary Antibody, Unconjugated
SKU/Catalog Number BA1039
Description This antibody is purified from antiserum by immunoaffinity chromatography which removes essentially all goat serum proteins, except the specific antibody for rabbit IgG. The antibody preparation is solid phase adsorbed with human serum proteins to ensure minimal cross reactivity in tissue or cell preparations.
Cite This Product Goat Anti-Rabbit IgG Secondary Antibody, Unconjugated (Boster Biological Technology, Pleasanton CA, USA, Catalog # BA1039)
Host Goat
Validated Species Rabbit
Application ELISA, IF, IHC, ICC, WB

*Our Boster Guarantee covers the use of this product in the above tested applications.

Immunogen Rabbit IgG (whole molecule).
Pack Size 1mg


Clonality Polyclonal
Storage At -20°C for 2 years. Avoid repeated freezing and thawing.


Secondary antibodies offer increased versatility enabling users to use many detection systems such as HRP, AP and fluorescence. They can also provide greater sensitivity through signal amplification as multiple secondary antibodies can bind to a single primary antibody, and secondary antibodies' FC regions provide further binding locations for biotin, enable the use of ABC and SABC to further amplify the signal. Most commonly, secondary antibodies are generated by immunizing the host animal with a pooled population of immunoglobulins from the target species. They are then purified through immunoaffinity chromatography and modified with antibody fragmentation, label conjugation, etc., to generate highly specific reagents.
Write a review for BA1039


Ye, Z., Ren, L., Tang, Z., Deng, Y., Xie, X., Fu, Z.,..., & Liu, E. (2017). Pulmonary C-fiber degeneration downregulates IFN-γ receptor 1 via IFN-α induction to attenuate RSV-induced airway hyperresponsiveness. Virology, 510, 262-272. doi: 10.1016/j.virol.2017.06.034
Gao, X., Dai, M., Li, Q., Wang, Z., Lu, Y., & Song, Z. (2017). HMGA2 regulates lung cancer proliferation and metastasis. Thoracic Cancer, 8(5), 501-510. doi: 10.1111/1759-7714.12476
Liu, Y., Xue, W., Zhu, L., Ye, D., Zhu, X., Wang, H.,..., & Deng, F. (2017). Nanog suppresses the expression of vasa by directly regulating nlk1 in the early zebrafish embryo. Biochimie, 142, 93-101. doi: 10.1016/j.biochi.2017.07.014
Mao, B., Liu, N., Yang, L., Xu, G., & Ye, S. (2017). Protein kinase D1 (PKD1) promotes angiogenesis following myocardial infarction via vascular endothelial growth factor (VEGF) pathway. International Journal of Clinical and Experimental Medicine, 10(7), 10528-10534. Retrieved from
Xu, T., Yu, X., Wang, T., Liu, Y., Liu, X., Ou, S., & Chen, Y. (2017). The effect of CXCR2 inhibition on seizure activity in the pilocarpine epilepsy mouse model. Brain Research Bulletin, 134, 91-98. Advance online publication. doi: 10.1016/j.brainresbull.2017.07.003
Guang, M., Huang, B., Yao, Y., Zhang, L., Yang, B., & Gong, P. (2017). Effects of vascular endothelial growth factor on osteoblasts around dental implants in vitro and in vivo. Journal of Oral Science, 59(2), 215-223. doi: 10.2334/josnusd.16-0406
Niu, K., Li, Y., Bai, R., Qu, Y., & Song, Y. (2017). Anion-exchange reactions: facile and general access to sensitive photoelectrochemical platforms for biomarker immunosensing. Journal of Materials Chemistry B. Advance online publication. doi: 10.1039/C7TB00998D
Li, Y., He, S., Tang, J., Ding, N., Chu, X., Cheng, L.,…, & Wu, J. (2017). Andrographolide Inhibits Inflammatory Cytokines Secretion in LPS-Stimulated RAW264.7 Cells through Suppression of NF-κB/MAPK Signaling Pathway. Evidence-Based Complementary and Alternative Medicine, 1-9. doi: 10.1155/2017/8248142