Recombinant human Raf1 (mutated Y340D + Y341D) protein (Active) (ab271473)
Key features and details
- Expression system: Baculovirus infected Sf9 cells
- Purity: >= 75% SDS-PAGE
- Active: Yes
- Tags: GST tag N-Terminus
- Suitable for: Functional Studies, SDS-PAGE
製品の詳細
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製品名
Recombinant human Raf1 (mutated Y340D + Y341D) protein (Active)
Raf1 タンパク質・ペプチド 製品一覧 -
生理活性
Specific activity = 200 pmol/min/µg.
Assay was done in a kinase buffer containing 1 mM DTT using MEK1 (0.1 mg/ml) as a substrate with 5 µM ATP at 30°C for 30 min.
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精製度
>= 75 % SDS-PAGE. -
発現系
Baculovirus infected Sf9 cells -
アクセッション番号
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タンパク質長
Protein fragment -
Animal free
No -
由来
Recombinant -
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生物種
Human -
予測される分子量
65 kDa including tags -
領域
306 to 648 -
修飾
mutated Y340D + Y341D -
タグ
GST tag N-Terminus -
配列の追加情報
Genbank: NM_002880
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特性
Our Abpromise guarantee covers the use of ab271473 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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アプリケーション
Functional Studies
SDS-PAGE
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製品の状態
Liquid -
Concentration information loading...
前処理および保存
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保存方法および安定性
Shipped on Dry Ice. Store at -80°C. Avoid freeze / thaw cycle.
pH: 8.00
Constituents: 0.63% Tris HCl, 0.64% Sodium chloride, 0.02% Potassium chloride, 0.05% (R*,R*)-1,4-Dimercaptobutan-2,3-diol, 20% Glycerol (glycerin, glycerine)This product is an active protein and may elicit a biological response in vivo, handle with caution.
関連情報
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別名
- c Raf
- C-raf
- C-Raf proto-oncogene, serine/threonine kinase
see all -
機能
Involved in the transduction of mitogenic signals from the cell membrane to the nucleus. Part of the Ras-dependent signaling pathway from receptors to the nucleus. Protects cells from apoptosis mediated by STK3. -
組織特異性
In skeletal muscle, isoform 1 is more abundant than isoform 2. -
関連疾患
Defects in RAF1 are the cause of Noonan syndrome type 5 (NS5) [MIM:611553]. Noonan syndrome (NS) is a disorder characterized by dysmorphic facial features, short stature, hypertelorism, cardiac anomalies, deafness, motor delay, and a bleeding diathesis. It is a genetically heterogeneous and relatively common syndrome, with an estimated incidence of 1 in 1000-2500 live births.
Defects in RAF1 are the cause of LEOPARD syndrome type 2 (LEOPARD2) [MIM:611554]. LEOPARD syndrome is an autosomal dominant disorder allelic with Noonan syndrome. The acronym LEOPARD stands for lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonic stenosis, abnormalities of genitalia, retardation of growth, and deafness. -
配列類似性
Belongs to the protein kinase superfamily. TKL Ser/Thr protein kinase family. RAF subfamily.
Contains 1 phorbol-ester/DAG-type zinc finger.
Contains 1 protein kinase domain.
Contains 1 RBD (Ras-binding) domain. -
翻訳後修飾
Phosphorylated upon DNA damage, probably by ATM or ATR. Phosphorylation at Thr-269 increases its kinase activity. Phosphorylation at Ser-259 induces the interaction with YWHAZ and inactivates kinase activity. Dephosphorylation of Ser-259 by the complex containing protein phosphatase 1, SHOC2 and M-Ras/MRAS relieves inactivation, leading to stimulate RAF1 activity. -
細胞内局在
Cytoplasm. Cell membrane. Colocalizes with RGS14 and BRAF in both the cytoplasm and membranes. - Information by UniProt
画像
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Functional Studies - Recombinant Human Raf1 protein (Tagged) (ab271473)
Functional analysis of ab271473.
Specific activity = 200 pmol/min/µg.
Assay was done in a kinase buffer containing 1 mM DTT using MEK1 (0.1 mg/ml) as a substrate with 5 µM ATP at 30°C for 30 min.
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SDS-PAGE - Recombinant Human Raf1 protein (Tagged) (ab271473)SDS-PAGE analysis of ab271473.
プロトコール
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
データシートおよび資料
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SDS download
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Datasheet download
参考文献 (0)
ab271473 は論文での使用が確認できていません。