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Kdm4c

Manufactured by Novus Biologicals
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KDM4C is a protein that functions as a histone demethylase. It is responsible for removing methyl groups from specific lysine residues on histone proteins, which can influence gene expression and chromatin structure.

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Lab products found in correlation

Kdm4a, by Novus Biologicals (2 mentions) Enhanced chemiluminescence, by Thermo Fisher Scientific (1 mentions) β actin, by Cell Signaling Technology (1 mentions) Kdm4d, by Abcam (1 mentions) C myc, by Santa Cruz Biotechnology (1 mentions) P27kip1, by Santa Cruz Biotechnology (1 mentions) Rnf20, by Proteintech (1 mentions) Nf κb2, by Proteintech (1 mentions) Jmjd6, by Proteintech (1 mentions) Kdm5a, by Proteintech (1 mentions) Nf κb p65, by Proteintech (1 mentions)

Close spelling variants of this product

Anti-KDM4C NBP1–49600 (2 citations)

2 protocols using kdm4c

1

Western Blot Analysis of Epigenetic Regulators

Cited 1 time
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For Western blot assays, conducted as previously described [7 (link)], antibodies against the following proteins were used: KDM4A (Novus, Littleton, CO, USA, NB110–40585), KDM4B (Bethyl Laboratories, Montgomery, TX, USA, A301–478A), KDM4C (Novus, NBP1–49600), KDM4D (Abcam, Hong Kong, China, ab198209), AR (Santa Cruz, sc-7305), histone H3 trimethyllysine 9 (H3K9me3) (Abcam, ab8898), histone H3 trimethyl lysine 4 (H3K4me3) (Abcam, ab8580), H3 (Abcam, ab1791), c-myc (Santa Cruz, sc-789), and p27kip1 (Santa Cruz, sc-508). Protein bands were visualized by enhanced chemiluminescence (Pierce Biotechnology, Rockford, IL, USA), and protein expression was normalized against β-actin (Cell Signaling Technology, Danvers, MA, USA).
Qiu M.T., Fan Q., Zhu Z., Kwan S.Y., Chen L., Chen J.H., Ying Z.L., Zhou Y., Gu W., Wang L.H., Cheng W.W., Zeng J., Wan X.P., Mok S.C., Wong K.K, & Bao W. (2015). KDM4B and KDM4A promote endometrial cancer progression by regulating androgen receptor, c-myc, and p27kip1. Oncotarget, 6(31), 31702-31720.
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2

Antibody Sources for Protein Studies

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Specific antisera were obtained from the following sources: HIV-1 Tat (ab42359 & ab43014), GFP (sc-9996), HA (Sigma, H9658-.2ML, clone HA-7 & Novus, NB600363), Flag (ThermoSientific, MA1-91878-1MG, clone FG4R), RNAPII-CTD (sc-56767, clone 8WG16), RNAPII CTD-Ser2P (Bethyl, A300-654A), RNAPII CTD-Ser5P (Active Motif, 39749), RNAPII CTD-Ser7P (Millipore, 04–1570), NF-κB/p65 (sc-372), NF-κB2 (ProteinTech, 10409-2-AP), H2B (Millipore, 07–371), H3 (Millipore, 05–928), TBP (sc-273), TAF4 (sc-136093), Cyclin T1 (sc-10750), CDK9 (sc-8338), RNF20 (ProteinTech, 21625-1-AP), KDM4A (Novus, NB110-40585), KDM4B (Novus, NB100-74605), KDM4C (NBP1-49600), KDM4D (NBP1-03357), KDM5A (NB110-40499), KDM5B (NB100-97821), JMJD6 (NBP1-71693), NELF-A (sc-32911), Csn3 (sc-100693), Csn8 (sc-393482), PRMT6 (ProteinTech, 15395-1-AP), SHMT1 (ProteinTech, 14149-1-AP), SHMT2 (ProteinTech, 11099-1-AP), BRCC36 (Novus, NBP1-76831), Ubquitin (Millipore, 05–944), K48Ub (Millipore, 05–1307), K63Ub (Millipore, 05–1313), p62 (ProteinTech, 18420-1-AP), Rabbit IgG (sc-2027), Mouse IgG (sc-2025) and HRP-conjugated 2nd antibodies (sc-2004, sc-2005 & sc-2033).
Xu M., Moresco J.J., Chang M., Mukim A., Smith D., Diedrich J.K., Yates JR I.I.I, & Jones K.A. (2018). SHMT2 and the BRCC36/BRISC deubiquitinase regulate HIV-1 Tat K63-ubiquitylation and destruction by autophagy. PLoS Pathogens, 14(5), e1007071.
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