1. 抗体
  2. 一抗
  3. 单克隆抗体 重组抗体
  4. SAM68 抗体 (YA2136)

SAM68 抗体 (YA2136)

目录号: HY-P82391
COA 抗体使用指南 技术支持

SAM68 Antibody (YA2136) 是一个兔来源、无偶联标记、抗 SAM68 的 IgG 单克隆抗体。

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规格 价格 是否有货 数量
10 μL ¥470 In-stock
50 μL ¥1220 In-stock
100 μL ¥2000 In-stock
250 μL   询价  

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【WB: 蛋白质免疫印迹; IHC-P: 石蜡切片样本的免疫组织化学; IHC-F: 冰冻切片样本的免疫组织化学; ICC/IF: 细胞免疫荧光; IF-Tissue: 组织免疫荧光; mIHC: 多重荧光免疫组化; IP: 免疫沉淀; ChIP: 染色质免疫沉淀; FC: 流式细胞术; ELISA: 酶联免疫吸附试验】

  • 生物活性

  • 技术参数

  • 产品性质

  • 产品资料

描述

SAM68 Antibody (YA2136) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to SAM68.

研究背景

SAM68 是一种 RNA 结合蛋白,参与多种受体系统(如 T 细胞、瘦素和胰岛素受体)的招募和酪氨酸磷酸化。磷酸化后,它通过结合含 SH2 和 SH3 结构域的蛋白质,在信号转导级联中充当适配蛋白。在细胞周期中,SAM68 参与 G2-M 期进程,并通过竞争性结合 CBP 抑制 CBP 依赖性转录激活。此外,它作为 mRNA 稳定性和/或翻译速率的潜在调节因子,介导 mRNA 核输出,并促进含组成型转运元件(CTE)的 mRNA 与大聚核糖体的结合及翻译起始。然而,有研究表明 SAM68 不参与未剪接 CTE 含 RNA 的核质输出。SAM68 还调控选择性剪接,影响 mRNA 剪接位点选择和外显子包含,特异性结合含 5'-[AU]UAA-3' 双部分基序(间隔超过 15 个核苷酸)的 RNA 及 poly(A)。在 Ras 通路依赖的方式下调控 CD44 选择性剪接,并与 HNRNPA1 协同调控 BCL2L1(促进 Bcl-X(S) 亚型生成)和 SMN1 的选择性剪接。在神经元活动依赖性方式下,与 KHDRBS2/SLIM-1 协同调控 NRXN1 和 NRXN3 在层粘连蛋白 G 样结构域 6 中的选择性剪接(含进化保守的 AS4 片段),但对 NRXN3 的调控表现为拮抗作用(By similarity)。亚型 3 仅在生长停滞细胞中表达,抑制 S 期进程。

基因 ID
蛋白数据库
中文名
SAM68 抗体 (YA2136)
同用名
Khdrbs1; p62; p68; Sam68
分子量

Predicted band size: 48 kDa; Observed band size: 68 kDa

纯度

Affinity Chromatography

偶联

Non-conjugated

修饰

Unmodified

RRID
研究领域

Signal Transduction

产品类别

Primary Antibody; Recombinant Rabbit Monoclonal Antibody

克隆性

Recombinant, Monoclonal

宿主

Rabbit

反应物种

Human, Mouse, Rat

推荐稀释比例

WB: 1:500-1:1000; IHC: 1:50-1:100; IF: 1:50-1:200

  • Western blot analysis of extracts from Hela (lane 2(20μg), Hela (lane 3(40μg), using SAM68 Antibody. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in TBST for 2 hour at room temperature. The primary antibody and Loading control antibody (Beta Actin, HY-P80438, 1/3000) was used in 5% BSA in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (HY-P8004/HY-P8001, 1/10,000) was used for 1 hour at room temperature.
  • Immunocytochemistry analysis of Hela cells labeling SAM68 with SAM68 Antibody (HY-P82391) at 1/50 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 for 10 minutes at room temperature, then blocked with QuickBlock™ Blocking Buffer for Immunol Staining for 10 min at room temperature. Cells were then incubated with SAM68 Antibody (HY-P82391) at 1/50 dilution in QuickBlock™ Blocking Buffer for Immunol Staining at 4 ℃. Alexa Fluor® 488-conjugated AffiniPure Goat Anti-Rabbit IgG H&L(HY-P8002, Green) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. The Nuclear counterstain was DAPI (Blue).
  • Immunocytochemistry analysis of NIH3T3 cells labeling SAM68 with SAM68 Antibody (HY-P82391) at 1/50 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 for 10 minutes at room temperature, then blocked with QuickBlock™ Blocking Buffer for Immunol Staining for 10 min at room temperature. Cells were then incubated with SAM68 Antibody (HY-P82391)at 1/50 dilution in QuickBlock™ Blocking Buffer for Immunol Staining at 4 ℃. Alexa Fluor® 488-conjugated AffiniPure Goat Anti-Rabbit IgG H&L(HY-P8002,Green) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. The Nuclear counterstain was DAPI (Blue).
  • Immunohistochemical analysis of paraffin-embedded mouse kidney tissue using SAM68 Antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 8 minutes. The tissues were blocked in QuickBlock for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody at 1/100 dilution in 4℃ overnight. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
  • Immunohistochemical analysis of paraffin-embedded mouse kidney tissue using SAM68 Antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 8 minutes. The tissues were blocked in QuickBlock for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody at 1/100 dilution in 4℃ overnight. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
应用

WB, IHC-P, ICC/IF

性状

液体

组分

Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA.

保存条件 & 期限

Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.

运输条件

Shipping with blue ice.

同型

IgG

敏感性

Endogenous

免疫原

A synthesized peptide derived from human SAM68

数据库
文件资料
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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SAM68 Antibody (YA2136)
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HY-P82391
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