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Anti-Ubiquitin Activating Enzyme E1/UBA1 Antibody (1K888)

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产品编号 TMAY-02188

Anti-Ubiquitin Activating Enzyme E1/UBA1 Antibody (1K888) 是一种 Mouse 抗体,靶向 Ubiquitin Activating Enzyme E1/UBA1。Anti-Ubiquitin Activating Enzyme E1/UBA1 Antibody (1K888) 可用于 ELISA,IP。

Anti-Ubiquitin Activating Enzyme E1/UBA1 Antibody (1K888)

Anti-Ubiquitin Activating Enzyme E1/UBA1 Antibody (1K888)

Rating icon 还可以
产品编号 TMAY-02188

Anti-Ubiquitin Activating Enzyme E1/UBA1 Antibody (1K888) 是一种 Mouse 抗体,靶向 Ubiquitin Activating Enzyme E1/UBA1。Anti-Ubiquitin Activating Enzyme E1/UBA1 Antibody (1K888) 可用于 ELISA,IP。

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产品介绍

生物活性
产品描述
Anti-Ubiquitin Activating Enzyme E1/UBA1 Antibody (1K888) is a Mouse antibody targeting Ubiquitin Activating Enzyme E1/UBA1. Anti-Ubiquitin Activating Enzyme E1/UBA1 Antibody (1K888) can be used in ELISA,IP.
Ig Type
Monoclonal Mouse IgG1
克隆号
1K888
交叉反应
Human
验证活性
UBA1 was immunoprecipitated using:

-Lane A:0.5 mg Hela Whole Cell Lysate.

-Lane B:0.5 mg K562 Whole Cell Lysate

-0.5 µL anti-UBA1 mouse monoclonal antibody and 60 μg of Immunomagnetic beads Protein G.

-Primary antibody:

-Anti-UBA1 mouse monoclonal antibody, at 1:500 dilution.

-Secondary antibody:

-Dylight 800-labeled antibody to Mouse IgG (H+L), at 1:7500 dilution.

-Developed using the odyssey technique.

-Performed under reducing conditions.

-Predicted band size: 111 kDa.

-Observed band size: 111 kDa
应用
ELISA,IP
推荐剂量
ELISA: 1:5000-1:10000; IP: 0.2-1 μL/mg of lysate
抗体种类
Monoclonal
宿主来源Mouse
构建方式This antibody was produced from a hybridoma resulting from the fusion of a mouse myeloma with B cells obtained from a mouse immunized with purified, recombinant Human UBE1 / UBA1 (rh UBE1 / UBA1; TMPY-02840; NP_003325.2; Ser2-Arg1058). The IgG fraction of the cell culture supernatant was purified by Protein A affinity chromatography.
纯化方式Protein A
性状Liquid
缓冲液0.2 μm filtered solution in PBS with 10% Trehalose, pH7.0
研究背景UBE1, also known as UBA1, belongs to the ubiquitin-activating E1 family. UBE1 gene complements an X-linked mouse temperature-sensitive defect in DNA synthesis, and thus may function in DNA repair. It is part of a gene cluster on chromosome Xp11.23. UBE1 catalyzes the first step in ubiquitin conjugation to mark cellular proteins for degradation. It also catalyzes the first step in ubiquitin conjugation to mark cellular proteins for degradation by first adenylating its C-terminal glycine residue with ATP, and thereafter linking this residue to the side chain of a cysteine residue in E1, yielding a ubiquitin-E1 thioester and free AMP. Defects in UBA1 can cause spinal muscular atrophy X-linked type 2 (SMAX2), also known as X-linked lethal infantile spinal muscular atrophy, distal X-linked arthrogryposis multiplex congenita or X-linked arthrogryposis type 1 (AMCX1). Spinal muscular atrophy refers to a group of neuromuscular disorders characterized by degeneration of the anterior horn cells of the spinal cord, leading to symmetrical muscle weakness and atrophy. SMAX2 is a lethal infantile form presenting with hypotonia, areflexia, and multiple congenital contractures.
偶联与修饰
偶联
Unconjugated
抗原信息
免疫原
Recombinant Human UBE1 / UBA1 protein (TMPY-02840)
抗原种属
Human
存储&运输
储存方式Store at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. Preservative-Free.
运输方式Shipping with blue ice.

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