arpc2 goat polyclonal (Abnova)
Structured Review

Arpc2 Goat Polyclonal, supplied by Abnova, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/arpc2 goat polyclonal/product/Abnova
Average 90 stars, based on 1 article reviews
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1) Product Images from "Tumor-associated autoantibodies from mouse breast cancer models are found in serum of breast cancer patients"
Article Title: Tumor-associated autoantibodies from mouse breast cancer models are found in serum of breast cancer patients
Journal: NPJ Breast Cancer
doi: 10.1038/s41523-021-00257-1
Figure Legend Snippet: Homology and function of selected antigens.
Techniques Used: Migration, Inhibition
Figure Legend Snippet: Four pooled siRNA knocked down expression of the targets VPS35 ( a , b ), ARPC2 ( c , d ), SERBP1 ( e , f ), KRT8 ( g , h ), and Pdia6 ( i , j ). Decreased expression of these proteins demonstrate decreased survival ( a , c , e , g , and i ) and increased apoptosis ( b , d , f , h , and j ) as compared to mock transfected in either triple negative (TNBC, HCC70) or HER2 positive (HER2, SKBR3) human breast cancer cell lines. Survival is measured as % survival compared to mock transfected cells and apoptosis is measured as fold increase compared to mock transfected calls. All studies are in triplicate. Error bars are standard error of mean (SEM) **** p < 0.0001, *** p < 0.001, ** p < 0.01, * p < 0.05.
Techniques Used: Expressing, Transfection
Figure Legend Snippet: Percent decreased tumor growth from TgMMTV-neu (light gray) and C3(1)Tag mice (dark gray) n = 8/group as compared to control PBS vaccinated mice (white). Mice were vaccinated with peptides from VPS35, ARPC2, SERBP1, KRT8, and PDIA6 or PBS with CFA/IFA adjuvant ~14 days for three times and then with 3 × 10 5 syngeneic mouse mammary tumor cells (MMC for TgMMTV-neu and M6 for C3(1)Tag) implanted. **** p < 0.0001.
Techniques Used: Control, Adjuvant
Figure Legend Snippet: Corrected spots per well (CSPW mean peptide wells as compared to no antigen wells using 3.5 × 10 5 cells/well) was correlated by linear regression with tumor volume (mm 3 ) for animals that received vaccination with pooled epitopes to a specific antigens and animals that received PBS controls. IFN-g immune response was evaluated by IFN-g ELISPOT. a VPS35, b ARPC2, c SERBP1, d KRT8, and e PDIA6. R 2 and p value shown in each panel.
Techniques Used: Enzyme-linked Immunospot
Figure Legend Snippet: Indirect ELISA of sera from women without breast atypia ( n = 43) was compared to sera from women undergoing breast surgery for mammographic abnormalities (benign pathology n = 12, hyperplasia n = 12, fibroadenoma n = 36, or DCIS n = 59), and women with known breast cancer ( n = 37). Y axis is ng/mL IgG antibody concentration by ELISA for each antigen and X axis is the breast pathology a VPS35, b ARPC2, c SERBP1, d KRT8, and e PDIA6 Error bars are standard error of mean (SEM) **** p < 0.0001, *** p < 0.001, ** p < 0.01, * p < 0.05.
Techniques Used: Indirect ELISA, Concentration Assay, Enzyme-linked Immunosorbent Assay