HMOX1 Antikörper (AA 1-30)

Produktnummer ABIN361697

Produktdetails anti-HMOX1 Antikörper

Target: HMOX1 (Heme Oxygenase (Decycling) 1 (HMOX1))

Bindungsspezifität: AA 1-30

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser HMOX1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC), Immunoprecipitation (IP), ELISA, Immunocytochemistry (ICC), Immunofluorescence (IF)

Spezifität: Detects 32 kDa. Does not cross-react with HO-2.

Kreuzreaktivität: Rind (Kuh), Hund, Meerschweinchen, Hamster, Human, Affe, Maus, Schwein, Kaninchen, Ratte

Aufreinigung: Protein G Purified

Immunogen: Human HO-1 synthetic peptide, amino acids 1-30

Klon: 1F12-A6

Isotyp: IgG1 kappa

Anwendungsinformationen

Applikationshinweise:

• WB (1:1000)
• IHC (1:100)
• ICC/IF (1:100)
• optimal dilutions for assays should be determined by the user.

Kommentare:

1 μg/ml was sufficient for detection of HO-1 in 10 μg of mixed human cell line lysate by colorimetric immunoblot analysis using Goat Anti-Mouse IgG:HRP as the secondary.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS pH 7.4, 50 % glycerol, 0.09 % sodium azide, Storage buffer may change when conjugated

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: -20°C

Referenzen für anti-HMOX1 Antikörper (ABIN361697)

Wang, Zhang, Xia, Zhang, Chen, Yang: "Protective effect of silencing Stat1 on high glucose-induced podocytes injury via Forkhead transcription factor O1-regulated the oxidative stress response." in: BMC molecular and cell biology, Vol. 20, Issue 1, pp. 27, (2020) (PubMed).

Kanzaki, Shinohara, Itohiya-Kasuya, Ishikawa, Nakamura: "Nrf2 activation attenuates both orthodontic tooth movement and relapse." in: Journal of dental research, Vol. 94, Issue 6, pp. 787-94, (2015) (PubMed).

Kanzaki, Shinohara, Kajiya, Fukaya, Miyamoto, Nakamura: "Nuclear Nrf2 induction by protein transduction attenuates osteoclastogenesis." in: Free radical biology & medicine, Vol. 77, pp. 239-48, (2014) (PubMed).

Al-Rifai, Rücker, Amslinger: "Opening or closing the lock? When reactivity is the key to biological activity." in: Chemistry (Weinheim an der Bergstrasse, Germany), Vol. 19, Issue 45, pp. 15384-95, (2013) (PubMed).

Details zu HMOX1

Target: HMOX1 (Heme Oxygenase (Decycling) 1 (HMOX1))

Andere Bezeichnung: HO-1 (HMOX1 Produkte)

Synonyme: HMOX1 antikoerper, ARABIDOPSIS THALIANA HEME OXYGENASE 1 antikoerper, ATHO1 antikoerper, F18A8.4 antikoerper, F18A8_4 antikoerper, GENOMES UNCOUPLED 2 antikoerper, GUN2 antikoerper, HEME OXYGENASE antikoerper, HEME OXYGENASE 1 antikoerper, HEME OXYGENASE 6 antikoerper, HO1 antikoerper, HY1 antikoerper, HY6 antikoerper, PLASTID HEME OXYGENASE antikoerper, REVERSAL OF THE DET PHENOTYPE 4 antikoerper, HO-1 antikoerper, wu:fc27c04 antikoerper, zgc:65984 antikoerper, D8Wsu38e antikoerper, Hemox antikoerper, Hmox antikoerper, Hsp32 antikoerper, HEOXG antikoerper, Heox antikoerper, Ho-1 antikoerper, Ho1 antikoerper, hsp32 antikoerper, MGC132176 antikoerper, Hmox1 antikoerper, HMOX1D antikoerper, HSP32 antikoerper, bK286B10 antikoerper, heme oxygenase 1 antikoerper, Plant heme oxygenase (decyclizing) family protein antikoerper, Heme oxygenase antikoerper, heme oxygenase antikoerper, heme oxygenase 1, chloroplastic antikoerper, heme oxygenase 1a antikoerper, heme oxygenase 1 L homeolog antikoerper, HMOX1 antikoerper, TED4 antikoerper, ho1 antikoerper, P9301_RS17555 antikoerper, A9601_RS17590 antikoerper, MAE_RS06565 antikoerper, HO1 antikoerper, hmox1a antikoerper, CPE0214 antikoerper, Cyan7425_2962 antikoerper, Hmox1 antikoerper, hmox1.L antikoerper, AM1_C0205 antikoerper, CC1G_11686 antikoerper, CpipJ_CPIJ007246 antikoerper

Hintergrund: Heme-oxygenase is a ubiquitous enzyme that catalyzes the initial and rate-limiting steps in heme catabolism yielding equimolar amounts of biliverdin, iron and carbon monoxide. Biliverdin is subsequently converted to bilirubin and the free iron is sequestered to ferritin (1). These products have important physiological effects as carbon monoxide is a potent vasodilator, biliverdin and bilirubin are potent antioxidants, and the free iron increases oxidative stress and regulates the expression of many mRNAs (2). There are three isoforms of heme-oxygenase, HO-1, HO-2 and HO-3, however HO-1 and HO-2 are the major isoforms as they both have been identified in mammals (3). HO-1, also known as heat shock protein 32, is an inducible isoform activated by most oxidative stress inducers, cytokines, inflammatory agents and heat shock. HO-2 is a constitutive isoform which is expressed under homeostatic conditions. HO-1 is also considered to be a cytoprotective factor in that free heme is highly reactive and cytotoxic, and secondly, carbon monoxide is a mediator inhibiting the inflammatory process and bilirubin is a scavenger for reactive oxygen, both of which are the end products of heme catalyzation (4). It has also been shown that HO-1 deficiency may cause reduced stress defense, a pro-inflammatory tendency (5), susceptibility to atherosclerotic lesion formation (6), endothelial cell injury, and growth retardation (7). Up-regulation of HO-1 is therefore said to be one of the major defense mechanisms of oxidative stress (4).

Gen-ID: 3162

NCBI Accession: NP_002124

UniProt: P09601

Pathways: Transition Metal Ion Homeostasis, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process, Production of Molecular Mediator of Immune Response, SARS-CoV-2 Protein Interaktom