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由来生物
mouse
品質水準
抗体製品の状態
ascites fluid
抗体製品タイプ
primary antibodies
クローン
ST2541, monoclonal
交差性
human
メーカー／製品名
Chemicon®
テクニック
ELISA: suitable
affinity binding assay: suitable
neutralization: suitable
western blot: suitable
アイソタイプ
IgG1
NCBIアクセッション番号
UniProtアクセッション番号
輸送温度
dry ice
ターゲットの翻訳後修飾
unmodified
遺伝子情報
human ... IFNA2(3440)
詳細
Interferon alpha-2 (UniProt P01563; also known as IFN-alpha-2, Interferon alpha-A, LeIF A) is encoded by the IFNA2 (also known as IFNA2A, IFNA2B, IFNA2C) gene (Gene ID 3440) in human. Interferons (IFNs) are cytokines whose prouction and release by host cells are induced in the presence of pathogens (e.g. viruses, bacteria, parasites) and tumor cells. Originally named for their ability to interfere with viral replication, IFNs mediate the activate immune cells, such as natural killer cells and macrophages, and increase host defense by up-regulating antigen presentation by boosting the expression of major histocompatibility complex (MHC) antigens. More than twenty distinct IFN genes and proteins have been identified and classified into three main types. Type I IFNs (IFN-α, IFN-β, IFN-ε, IFN-κ, and IFN-ω) exert their function via binding IFN-α/β receptor (encoded by the IFNAR1 and IFNAR2 gene, respectively). IFN-γ is the only known type II IFN, it is released by type 1 T helper cells and binds IFN-γ receptor (encoded by the IFNGR1 and IFNGR2 gene, respectively). Type III IFNs signal through a receptor complex consisting of IL10R2 (CRF2-4) and IFNLR1 (CRF2-12).
特異性
Clone ST2541 neutralized human IFN-αA (IFN-α2) and IFN-αN (produced by Nalmalwa human Burkitt′s lymphoma cells), but not IFN-α1, antiviral activity (Shearer, M., et al. (1984). J. Immunol. 133(6):3096-3101).
免疫原
Human alpha-interferon.
アプリケーション
Research Category
炎症及び免疫
炎症及び免疫
Research Sub Category
サイトカイン及びサイトカイン受容体
サイトカイン及びサイトカイン受容体
Detect Interferon-α2 using this Anti-Interferon-α2 Antibody, clone ST254 validated for use in NEUT, WB, ELISA, Affinity binding.
Neutralizing Analysis: A representative lot enhanced viral replication by neutralizing host-secreted IFN in human prostate cancer PC3 cultures infected with P/V-CPI(−) and P/V-CPI(−)-G3A at a low MOI (Gainey, M.D., et al. (2000). J. Virol. 82(19):9369-9380).
Neutralizing Analysis: A representative lot neutralized human IFN-αA (IFN-α2) and IFN-αN (produced by Nalmalwa human Burkitt′s lymphoma cells), but not IFN-α1, antiviral activity against Semliki Forest Virus in human WISH amniotic epithelial cell cultures (Shearer, M., et al. (1984). J. Immunol. 133(6):3096-3101).
Affinity Binding Assay: A representative lot captured human IFN-α2, but not human IFN-α1 (Shearer, M., et al. (1984). J. Immunol. 133(6):3096-3101).
ELISA Neutralizing Analysis: A representative lot was used as the detection antibody for the detection of human IFN-αN (produced by Nalmalwa human Burkitt′s lymphoma cells) by sandwich ELISA (Shearer, M., et al. (1984). J. Immunol. 133(6):3096-3101).
Western Blotting Analysis: A representative lot detected IFN-αA (IFN-α2) and IFN-αN (produced by Nalmalwa human Burkitt′s lymphoma cells) under reducing condition by Western blotting (Shearer, M., et al. (1984). J. Immunol. 133(6):3096-3101).
Neutralizing Analysis: A representative lot neutralized human IFN-αA (IFN-α2) and IFN-αN (produced by Nalmalwa human Burkitt′s lymphoma cells), but not IFN-α1, antiviral activity against Semliki Forest Virus in human WISH amniotic epithelial cell cultures (Shearer, M., et al. (1984). J. Immunol. 133(6):3096-3101).
Affinity Binding Assay: A representative lot captured human IFN-α2, but not human IFN-α1 (Shearer, M., et al. (1984). J. Immunol. 133(6):3096-3101).
ELISA Neutralizing Analysis: A representative lot was used as the detection antibody for the detection of human IFN-αN (produced by Nalmalwa human Burkitt′s lymphoma cells) by sandwich ELISA (Shearer, M., et al. (1984). J. Immunol. 133(6):3096-3101).
Western Blotting Analysis: A representative lot detected IFN-αA (IFN-α2) and IFN-αN (produced by Nalmalwa human Burkitt′s lymphoma cells) under reducing condition by Western blotting (Shearer, M., et al. (1984). J. Immunol. 133(6):3096-3101).
物理的形状
Liquid, no preservatives
保管および安定性
Store at -20°C for up to one year. Avoid repeated freeze/thaw cycles.
法的情報
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
免責事項
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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保管分類コード
10 - Combustible liquids
WGK
WGK 1
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
MAB411:
試験成績書（COA）
製品のロット番号・バッチ番号を入力して、試験成績書（COA） を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
Innate immune signaling induces high levels of TC-specific deaminase activity in primary monocyte-derived cells through expression of APOBEC3A isoforms.
Thielen, BK; McNevin, JP; McElrath, MJ; Hunt, BV; Klein, KC; Lingappa, JR
The Journal of Biological Chemistry null
Monoclonal antibodies that distinguish between subspecies of human interferon-alpha and that detect interferon oligomers.
Shearer, M, et al.
Journal of immunology (Baltimore, Md. : 1950), 133, 3096-3101 (1984)
Jonathan C Reed et al.
The Journal of cell biology, 198(3), 439-456 (2012-08-02)
To produce progeny virus, human immunodeficiency virus type I (HIV-1) Gag assembles into capsids that package the viral genome and bud from the infected cell. During assembly of immature capsids, Gag traffics through a pathway of assembly intermediates (AIs) that
A hyperfusogenic F protein enhances the oncolytic potency of a paramyxovirus simian virus 5 P/V mutant without compromising sensitivity to type I interferon.
Gainey, MD; Manuse, MJ; Parks, GD
Journal of virology null
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