Kdm6b Antikörper (N-Term)

Produktnummer ABIN387862

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch Kdm6b in WB, IF und IHC (p). Er zeigt eine Reaktivität gegenüber Human und wurde in 15+ Publikationen erwähnt.

Kurzübersicht für Kdm6b Antikörper (N-Term) (ABIN387862)

Target: Kdm6b (Lysine (K)-Specific Demethylase 6B (Kdm6b))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Kdm6b Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Klon: RB10077

Produktdetails anti-Kdm6b Antikörper

Bindungsspezifität: AA 1-30, N-Term

Homologie: M

Aufreinigung: This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

Immunogen: This JMJD3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human JMJD3.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: IF: 1:10~50. WB: 1:1000. IHC-P: 1:10~50

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handhabung: Avoid freeze-thaw cycles.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots.

Haltbarkeit: 6 months

Referenzen für anti-Kdm6b Antikörper (ABIN387862)

Angrisano, Pero, Brancaccio, Coretti, Florio, Pezone, Calabrò, Falco, Keller, Lembo, Avvedimento, Chiariotti: "Cyclical DNA Methylation and Histone Changes Are Induced by LPS to Activate COX-2 in Human Intestinal Epithelial Cells." in: PLoS ONE, Vol. 11, Issue 6, pp. e0156671, (2017) (PubMed).

Petruk, Mariani, De Dominici, Porazzi, Minieri, Cai, Iacovitti, Flomenberg, Calabretta, Mazo: "Structure of Nascent Chromatin Is Essential for Hematopoietic Lineage Specification." in: Cell reports, Vol. 19, Issue 2, pp. 295-306, (2017) (PubMed).

Liao, Kuo, Lu, Wang, Wu: "Generation of an anti-EpCAM antibody and epigenetic regulation of EpCAM in colorectal cancer." in: International journal of oncology, Vol. 46, Issue 4, pp. 1788-800, (2015) (PubMed).

Hashizume, Andor, Ihara, Lerner, Gan, Chen, Fang, Huang, Tom, Ngo, Solomon, Mueller, Paris, Zhang, Petritsch, Gupta, Waldman, James: "Pharmacologic inhibition of histone demethylation as a therapy for pediatric brainstem glioma." in: Nature medicine, (2014) (PubMed).

Lee, Na, Lee, Na, Cho, Wu, Yune, Kim, Ju: "Molecular mechanism of Jmjd3-mediated interleukin-6 gene regulation in endothelial cells underlying spinal cord injury." in: Journal of neurochemistry, Vol. 122, Issue 2, pp. 272-82, (2013) (PubMed).

Ramadoss, Chen, Wang: "Histone demethylase KDM6B promotes epithelial-mesenchymal transition." in: The Journal of biological chemistry, Vol. 287, Issue 53, pp. 44508-17, (2012) (PubMed).

Balasubramanian, Chew, Eckert: "Sulforaphane suppresses polycomb group protein level via a proteasome-dependent mechanism in skin cancer cells." in: Molecular pharmacology, Vol. 80, Issue 5, pp. 870-8, (2011) (PubMed).

Hyland, McDade, McCloskey, Dickson, Arthur, McCance, Patel: "Evidence for alteration of EZH2, BMI1, and KDM6A and epigenetic reprogramming in human papillomavirus type 16 E6/E7-expressing keratinocytes." in: Journal of virology, Vol. 85, Issue 21, pp. 10999-1006, (2011) (PubMed).

Kim, Yoon, Chuong, Oyolu, Wills, Gupta, Baker: "Chromatin and transcriptional signatures for Nodal signaling during endoderm formation in hESCs." in: Developmental biology, Vol. 357, Issue 2, pp. 492-504, (2011) (PubMed).

Lu, Lu, Liao, Yu, Chung, Kao, Wu: "Epithelial cell adhesion molecule regulation is associated with the maintenance of the undifferentiated phenotype of human embryonic stem cells." in: The Journal of biological chemistry, Vol. 285, Issue 12, pp. 8719-32, (2010) (PubMed).

Dai, Lu, Zhang, Shen: "Jmjd3 activates Mash1 gene in RA-induced neuronal differentiation of P19 cells." in: Journal of cellular biochemistry, Vol. 110, Issue 6, pp. 1457-63, (2010) (PubMed).

Toth, Maglinte, Lee, Lee, Wong, Brulois, Lee, Buckley, Laird, Marquez, Jung: "Epigenetic analysis of KSHV latent and lytic genomes." in: PLoS pathogens, Vol. 6, Issue 7, pp. e1001013, (2010) (PubMed).

Peláez, Kalogeropoulou, Ferraro, Voulgari, Pankotai, Boros, Pintzas: "Oncogenic RAS alters the global and gene-specific histone modification pattern during epithelial-mesenchymal transition in colorectal carcinoma cells." in: The international journal of biochemistry & cell biology, Vol. 42, Issue 6, pp. 911-20, (2010) (PubMed).

Long, Huang, Yin, Zhao, Zhao, Lu: "Abnormal expression pattern of histone demethylases in CD4(+) T cells of MRL/lpr lupus-like mice." in: Lupus, Vol. 18, Issue 14, pp. 1327-8, (2009) (PubMed).

Ishii, Wen, Corsa, Liu, Coelho, Allen, Carson, Cavassani, Li, Lukacs, Hogaboam, Dou, Kunkel: "Epigenetic regulation of the alternatively activated macrophage phenotype." in: Blood, Vol. 114, Issue 15, pp. 3244-54, (2009) (PubMed).

Details zu Kdm6b

Target: Kdm6b (Lysine (K)-Specific Demethylase 6B (Kdm6b))

Andere Bezeichnung: JMJD3

Hintergrund: Covalent modification of histones plays critical role in regulating chromatin structure and transcription. While most covalent histone modifications are reversible, only recently has it been established that methyl groups are subject to enzymatic removal from histones. A family of novel JmjC domain-containing histone demethylation (JHDM) enzymes have been identified that perform this specific function. Histone demethylation by JHDM proteins requires cofactors Fe(II) and alpha-ketoglutarate. Family members include JHDM1 (demethylating histone 3 at lysine 36), and JHDM2A as well as JMJD2CH3K9 (both of which demethylate histone 3 at lysine 9). Contributions of histone demethylase activity to tumor development, decreases in cell proliferation, and hormone-dependent transcriptional activation have been observed.

Molekulargewicht: 176632

Gen-ID: 23135

NCBI Accession: NP_001073893

UniProt: O15054

Pathways: Warburg Effekt