抗EG-VEGF/PK1抗体(Anti-EG-VEGF/PK1, Goat-Poly, Biotin antibody)
掲載日情報:2021/01/28 現在Webページ番号:29075
EG-VEGF/PK1に対する抗体(Anti-EG-VEGF/PK1, 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
- Related Product & Information
価格
[在庫・価格 :2025年04月26日 20時35分現在]
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[在庫・価格 :2025年04月26日 20時35分現在]
Anti-EG-VEGF/PK1, Goat-Poly, Biotin
文献数: 0
- 商品コード:BAF1209
- メーカー:RSD
- 包装:50μg
- 価格:¥115,000
- 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 EG-VEGF/PK1 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#MAB12091,スタンダードとして#1209-EV-025を用いる。 別名:EGVEGF Genbank No: 84432 Protein Accession No: P58294 |
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法規制等 | |||
保存条件 | 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 | Myeloid-derived Suppressor Cell Marker |
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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 | Mouse myeloma cell line NS0-derived recombinant human EG‑VEGF/PK1 (R&D Systems, Catalog # 1209-EV)Ala20-Phe105Accession # P58294 |
Source | Polyclonal Goat IgG |
Purification | Antigen Affinity-purified |
Specificity | Detects human EG‑VEGF/PK1 in ELISAs and Western blots. In sandwich immunoassays, approximately 80% cross-reactivity with recombinant rat EG-VEGF is observed and 60% cross-reactivity with recombinant mouse EG-VEGF is observed. |
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Applications and Data
Recommended Concentration | Sample | |
Western Blot | 0.1 µg/mL | Recombinant Human EG-VEGF/PK1 (Catalog # 1209-EV) |
Human EG-VEGF/PK1 Sandwich Immunoassay | Reagent | |
ELISA Capture (Matched Antibody Pair) | 2-8 µg/mL | Human EG‑VEGF/PK1 Antibody (Catalog #MAB12091 ) |
ELISA Detection (Matched Antibody Pair) | 0.1-0.4 µg/mL | Human EG‑VEGF/PK1 Biotinylated Antibody (Catalog #BAF1209 ) |
ELISA Standard | Recombinant Human EG-VEGF/PK1 Protein (Catalog #1209-EV ) | |
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: EG-VEGF/PK1 | Endocrine gland-derived vascular endothelial growth factor (EG-VEGF), also called prokineticin 1 (PK1), is a member of the prokineticin family of secreted proteins that share a common structural motif containing ten conserved cysteine residues that form five pairs of disulfide bonds (1, 2). Members of this family include the mammalian EG-VEGF/PK1 and PK2, as well as the venom protein A (VPRA) from the venom of black mamba snake and the frog Bombina variegata, Bv8 (1). Human EG-VEGF precursor is a 105 amino acid (aa) residue protein with a 19 aa signal peptide that is cleaved to yield a 86 aa mature protein (1, 2). EG-VEGF is expressed in multiple tissues including the gastrointestinal (GI) tract and steroidogenic glands (testis, ovary, placenta and adrenal glands). EG-VEGF has been shown to potently stimulate the contraction of GI smooth muscle. In addition, EG-VEGF is a tissue-specific angiogenic factor that exhibits biological activities similar to that of VEGF on select cells. It induces the proliferation, migration, and fenestration in cultured endocrine gland-derived capillary endothelial cells. EG-VEGF binds to and activates two closely related G protein-coupled receptors, EG-VEGF/PK1-R1 and EG-VEGF/PK2-R2 (3, 4). Activation of the receptors leads to stimulation of phosphoinositide turnover and activation of p44/p42 MAP kinase signaling pathways. |
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References
Li, M. et al. (2001) Mol. Pharmacol. 59:692. | |
LeCouter, J. et al. (2001) Nature 412:877. | |
Lin, D. et al. (2002) J. Biol. Chem. 277:19276. | |
Masuda, Y. et al. (2002) Biochem. Biophys. Res. Commun. 293:396. | |
Long Name: | Endocrine Gland-derived Vascular Endothelial Growth Factor |
Entrez Gene IDs: | 84432 (Human); 246691 (Mouse); 192205 (Rat) |
Alternate Names: | EGVEGF; EG-VEGF; EGVEGFblack mamba toxin-related protein; Endocrine-gland-derived vascular endothelial growth factor; Mambakine; PK1mambakine; PRK1prokineticin-1; PROK1; Prokineticin 1 |
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Related Research Areas
Digestive Peptide Hormones and Regulators |
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Related Product & Information
Background | EG-VEGF/PK1 |
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background_content | Background: EG-VEGF/PK1 Endocrine gland-derived vascular endothelial growth factor (EG-VEGF), also called prokineticin 1 (PK1), is a member of the prokineticin family of secreted proteins that share a common structural motif containing ten conserved cysteine residues that form five pairs of disulfide bonds (1, 2). Members of this family include the mammalian EG-VEGF/PK1 and PK2, as well as the venom protein A (VPRA) from the venom of black mamba snake and the frog Bombina variegata, Bv8 (1). Human EG-VEGF precursor is a 105 amino acid (aa) residue protein with a 19 aa signal peptide that is cleaved to yield a 86 aa mature protein (1, 2). EG-VEGF is expressed in multiple tissues including the gastrointestinal (GI) tract and steroidogenic glands (testis, ovary, placenta and adrenal glands). EG-VEGF has been shown to potently stimulate the contraction of GI smooth muscle. In addition, EG-VEGF is a tissue-specific angiogenic factor that exhibits biological activities similar to that of VEGF on select cells. It induces the proliferation, migration, and fenestration in cultured endocrine gland-derived capillary endothelial cells. EG-VEGF binds to and activates two closely related G protein-coupled receptors, EG-VEGF/PK1-R1 and EG-VEGF/PK2-R2 (3, 4). Activation of the receptors leads to stimulation of phosphoinositide turnover and activation of p44/p42 MAP kinase signaling pathways. |
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