抗MIG抗体(Anti-MIG, Human, Goat-Poly, Biotin antibody)
掲載日情報:2021/01/28 現在Webページ番号:27631
MIGに対する抗体(Anti-MIG, Human, Goat-Poly, Biotin )です。
※ 本製品は研究用です。研究用以外には使用できません。
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- 価格
- Product Details
- Applications and Data
- References
- Related Research Areas
- Summary
- Related Product & Information
- Citations
価格
[在庫・価格 :2025年04月26日 20時35分現在]
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Anti-MIG, Human, Goat-Poly, Biotin |
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[在庫・価格 :2025年04月26日 20時35分現在]
Anti-MIG, Human, Goat-Poly, Biotin
文献数: 6
- 商品コード:BAF392
- メーカー:RSD
- 包装:50μg
- 価格:¥119,000
- 在庫:無(未発注)
- 納期:10日程度 ※※ 表示されている納期は弊社に在庫がなく、取り寄せた場合の目安納期となります。
- 法規制等:
説明文 | マッチドペア:Human CXCL9/MIG サンドイッチELISAの検出用抗体として利用可能,補足用抗体として#MAB392-500,スタンダードとして#392-MG-010を用いる。 別名:chemokine (C-X-C motif) ligand 9 Genbank No: 4283 Protein Accession No: Q07325 |
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保存条件 | -20℃ | 法規備考 | |
抗原種 | Human | 免疫動物 | Goat |
交差性 | Human | 適用 | ELISA,Western Blot |
標識 | Biotin | 性状 | Antigen Affinity Purified |
吸収処理 | クラス | IgG | |
クロナリティ | Polyclonal | フォーマット | |
掲載カタログ |
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製品記事 | |||
関連記事 | R&D Systems(R&Dシステムズ)社 ELISA用ペア抗体を使用したELISA 構築ガイド |
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Product Details
Species Reactivity | Human |
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Label | Biotin |
Immunogen | E. coli-derived recombinant human CXCL9/MIG (R&D Systems, Catalog # 392-MG)Thr23-Thr125Accession # Q07325 |
Source | Polyclonal Goat IgG |
Purification | Antigen Affinity-purified |
Specificity | Detects human CXCL9/MIG in ELISAs and Western blots. In sandwich immunoassays, less than 0.2% cross-reactivity with recombinant human (rh) IL‑12, recombinant mouse CXCL9/MIG, and rhIL‑8 is observed. |
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Applications and Data
Recommended Concentration | Sample | |
Western Blot | 0.1 µg/mL | Recombinant Human CXCL9/MIG (Catalog # 392-MG) |
Human CXCL9/MIG Sandwich Immunoassay | Reagent | |
ELISA Capture (Matched Antibody Pair) | 2-8 µg/mL | Human CXCL9/MIG Antibody (Catalog #MAB392 ) |
ELISA Detection (Matched Antibody Pair) | 0.1-0.4 µg/mL | Human CXCL9/MIG Biotinylated Antibody (Catalog #BAF392 ) |
ELISA Standard | Recombinant Human CXCL9/MIG Protein (Catalog #392-MG ) | |
Please Note: Optimal dilutions should be determined by each laboratory for each application.General Protocolsare available in the Technical Information section on our website. | Preparation and Storage | |
Reconstitution | Reconstitute at 0.2 mg/mL in sterile PBS. | Reconstitution Buffer Available |
Shipping | The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. | |
Stability & Storage | Use a manual defrost freezer and avoid repeated freeze-thaw cycles. 12 months from date of receipt, -20 to -70 °C as supplied. | |
1 month, 2 to 8 °C under sterile conditions after reconstitution. | ||
6 months, -20 to -70 °C under sterile conditions after reconstitution. | ||
Background: CXCL9/MIG | CXCL9, a member of the alpha subfamily of chemokines that lack the ELR domain, was initially identified as a lymphokine-activated gene in mouse macrophages. Human CXCL9 was subsequently cloned using mouse MIG cDNA as a probe. The CXCL9 gene is induced in macrophages and in primary glial cells of the central nervous system specifically in response to IFN-gamma. CXCL9 has been shown to be a chemoattractant for activated T-lymphocytes and TIL but not for neutrophils or monocytes. The human CXCL9 cDNA encodes a 125 amino acid residue precursor protein with a 22 amino acid residue signal peptide that is cleaved to yield a 103 amino acid residue mature protein. CXCL9 has an extended carboxy-terminus containing greater than 50% basic amino acid residues and is larger than most other chemokines. The carboxy-terminal residues of CXCL9 are prone to proteolytic cleavage resulting in size heterogeneity of natural and recombinant CXCL9. CXCL9 with large carboxy-terminal deletions have been shown to have diminished activity in the calcium flux assay. A chemokine receptor (CXCR3) specific for CXCL9 and IP‑10 has been cloned and shown to be highly expressed in IL-2-activated T-lymphocytes. |
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References
Loetscher, M. et al. (1996) J. Exp. Med. 184:963. | |
Liao, F. et al. (1995) J. Exp. Med. 182:1301. | |
Vanguri, P. (1995) J. Neuroimmunol. 56:35. | |
Entrez Gene IDs: | 4283 (Human); 17329 (Mouse); 246759 (Rat) |
Alternate Names: | chemokine (C-X-C motif) ligand 9; CMK; crg-10; C-X-C motif chemokine 9; CXCL9; Gamma-interferon-induced monokine; Humig; MIG; MIGSmall-inducible cytokine B9; monokine induced by gamma interferon; SCYB9Monokine induced by interferon-gamma |
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Related Research Areas
Cancer Biomarkers | ||||||||||
Chemokines and Receptors | ||||||||||
Chemokines and Receptors in Angiogenesis | ||||||||||
CXC Chemokines and Receptors | ||||||||||
Inflammatory Mediators | ||||||||||
Macrophage Activation Markers | ||||||||||
Molecules Secreted by VSMC | ||||||||||
Regulatory T Cells (Tregs) | ||||||||||
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Images | Ratings | Applications | Species | Reviewed By | Date | Details | ||||
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![]() Enlarge | Excellent | ELISA | Human | Anonymous | 12/06/2017 | Image Details |
![]() ELISA: Human CXCL9/MIG Biotinylated Antibody [BAF392]. |
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Summary
Application | ELISA |
Sample Tested | Serum and Plasma |
Species | Human |
Other Experimental Details | MAB392 was used as a capture in a sandwich ELISA for MIG. The detection antibody was BAM392. The standard was 392-MG-010. Sensitivity was around 5 pg/ml. |
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Related Product & Information
Background | CXCL9/MIG |
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background_content | Background: CXCL9/MIG CXCL9, a member of the alpha subfamily of chemokines that lack the ELR domain, was initially identified as a lymphokine-activated gene in mouse macrophages. Human CXCL9 was subsequently cloned using mouse MIG cDNA as a probe. The CXCL9 gene is induced in macrophages and in primary glial cells of the central nervous system specifically in response to IFN-gamma. CXCL9 has been shown to be a chemoattractant for activated T-lymphocytes and TIL but not for neutrophils or monocytes. The human CXCL9 cDNA encodes a 125 amino acid residue precursor protein with a 22 amino acid residue signal peptide that is cleaved to yield a 103 amino acid residue mature protein. CXCL9 has an extended carboxy-terminus containing greater than 50% basic amino acid residues and is larger than most other chemokines. The carboxy-terminal residues of CXCL9 are prone to proteolytic cleavage resulting in size heterogeneity of natural and recombinant CXCL9. CXCL9 with large carboxy-terminal deletions have been shown to have diminished activity in the calcium flux assay. A chemokine receptor (CXCR3) specific for CXCL9 and IP‑10 has been cloned and shown to be highly expressed in IL-2-activated T-lymphocytes. |
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Citations
- Upregulation of human cytomegalovirus by HIV type 1 in human lymphoid tissue ex vivo.
Authors: Biancotto A, Iglehart SJ, Lisco A, Vanpouille C, Grivel JC, Lurain NS, Reichelderfer PS, Margolis LB
AIDS Res. Hum. Retroviruses, 2008;24(3):453-62.
Species: Human
Sample Type: Cell Culture Supernates
Application: Luminex Development - Abnormal activation and cytokine spectra in lymph nodes of people chronically infected with HIV-1.
Authors: Biancotto A, Grivel JC, Iglehart SJ, Vanpouille C, Lisco A, Sieg SF, Debernardo R, Garate K, Rodriguez B, Margolis LB, Lederman MM
Blood, 2007;109(10):4272-9.
Species: Human
Sample Type: Cell Culture Supernates
Application: Luminex Development - Imbalance in the expression of CXC chemokines correlates with bronchoalveolar lavage fluid angiogenic activity and procollagen levels in acute respiratory distress syndrome.
Authors: Keane MP, Donnelly SC, Belperio JA, Goodman RB, Dy M, Burdick MD, Fishbein MC, Strieter RM
J. Immunol., 2002;169(11):6515-21.
Species: Human
Sample Type: BALF
Application: ELISA Development
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