WB result of IFIH1/MDA5 Mouse mAb
Primary antibody: IFIH1/MDA5 Mouse mAb at 1/1000 dilution
Lane 1: Jurkat whole cell lysate 20 µg
Lane 2: T-47D whole cell lysate 20 µg
Lane 3: Daudi whole cell lysate 20 µg
Lane 4: Raji whole cell lysate 20 µg
Secondary antibody: Goat Anti- mouse IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 117 kDa
Observed MW: 125 kDa
Product Details
Product Details
Product Specification
| Host | Mouse |
| Antigen | IFIH1/MDA5 |
| Synonyms | Interferon-induced helicase C domain-containing protein 1; Clinically amyopathic dermatomyositis autoantigen 140 kDa (CADM-140 autoantigen); Helicase with 2 CARD domains (Helicard); Interferon-induced with helicase C domain protein 1; Melanoma differentiation-associated protein 5 (MDA-5); Murabutide down-regulated protein; MDA5 s; RH116; IFIH1 |
| Location | Cytoplasm, Mitochondrion |
| Accession | Q9BYX4 |
| Antibody Type | Mouse mAb |
| Isotype | IgG1 |
| Application | WB, IHC-P, ICFCM |
| Reactivity | Hu |
| Positive Sample | Jurkat, T-47D, Daudi, Raji, THP-1 treated with LPS 1μg for 24 hours |
| Purification | Protein G |
| Concentration | 1 mg/ml |
| Conjugation | Unconjugated |
| Physical Appearance | Liquid |
| Storage Buffer | PBS, 40% Glycerol, 0.05% BSA, 0.02% sodium azide |
| Stability & Storage | 12 months from date of receipt / reconstitution, -20 °C as supplied |
Dilution
| application | dilution | species |
| WB | 1:1000-1:5000 | Hu |
| IHC-P | 1:500 | Hu |
| ICFCM | 1:400 | Hu |
Background
IFIH1, also known as melanoma differentiation-associated gene 5 (MDA5), is a critical viral nucleic acid sensor in the cytoplasm that acts as a "sentinel" in initiating the antiviral innate immune response. Its primary function is to recognize long double-stranded RNA (>1 kb) or mRNA lacking 2'-O-methylation at the 5' end that has invaded the cell. Upon binding to these virus-characteristic nucleic acids, IFIH1 forms polymers through homotypic interactions and associates with the mitochondrial adaptor protein MAVS, thereby activating downstream signaling pathways and ultimately inducing the production of type I interferons (such as IFN-α and IFN-β) and pro-inflammatory cytokines to eliminate the virus. Functionally, IFIH1 belongs to the RIG-I-like receptor family alongside RIG-I, but the two exhibit a division of labor in terms of the viral spectra they recognize—for example, IFIH1 is the key receptor responsible for detecting picornaviruses (such as encephalomyocarditis virus), coronaviruses (including SARS-CoV-2), and unspliced RNAs transcribed from HIV-1 proviruses. However, gain-of-function mutations in the IFIH1 gene can lead to aberrant activation of the type I interferon signaling pathway, thereby giving rise to a range of autoinflammatory and autoimmune diseases, such as Aicardi-Goutières syndrome type 7 (characterized by intracranial calcification, leukoencephalopathy, and chilblain-like rashes), Singleton-Merten syndrome, and type 1 diabetes mellitus.
Picture
Picture
Western Blot
WB result of IFIH1/MDA5 Mouse mAb
Primary antibody: IFIH1/MDA5 Mouse mAb at 1/1000 dilution
Lane 1: untreated THP-1 whole cell lysate 20 µg
Lane 2: THP-1 treated with LPS 1μg for 24 hours whole cell lysate 20 µg
Secondary antibody: Goat Anti- mouse IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 117 kDa
Observed MW: 125 kDa
Immunohistochemistry
IHC shows positive staining in paraffin-embedded human kidney. Anti-IFIH1 antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human liver. Anti-IFIH1 antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
