验证数据展示
经过测试的应用
Positive WB detected in | K-562 cells |
Positive IP detected in | K-562 cells |
推荐稀释比
应用 | 推荐稀释比 |
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Western Blot (WB) | WB : 1:500-1:2000 |
Immunoprecipitation (IP) | IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate |
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Sample-dependent, Check data in validation data gallery. |
产品信息
24555-1-AP targets TRAPPC12 in WB, IP, ELISA applications and shows reactivity with human samples.
经测试应用 | WB, IP, ELISA Application Description |
经测试反应性 | human |
免疫原 | TRAPPC12 fusion protein Ag18332 种属同源性预测 |
宿主/亚型 | Rabbit / IgG |
抗体类别 | Polyclonal |
产品类型 | Antibody |
全称 | tetratricopeptide repeat domain 15 |
别名 | TTC15, CGI 87, CGI-87, TPR repeat protein 15, Trafficking of membranes and mitosis |
计算分子量 | 735 aa, 79 kDa |
观测分子量 | 98 kDa |
GenBank蛋白编号 | BC014164 |
基因名称 | TRAPPC12 |
Gene ID (NCBI) | 51112 |
偶联类型 | Unconjugated |
形式 | Liquid |
纯化方式 | Antigen affinity purification |
UNIPROT ID | Q8WVT3 |
储存缓冲液 | PBS with 0.02% sodium azide and 50% glycerol, pH 7.3. |
储存条件 | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
背景介绍
TRAPPC12, also called CGI-87, TTC15 and TRAMM, has been recently identified as subunit of TRAPP complex in two independent proteomic studies. It was suggested that TRAPPC12 was a subunit of TRAPPIII. TRAPPC12 and TECPR1 acted at distinct steps in autophagy and depletion of TRAPPC12 and/or TECPR1 increased in the number of autophagosomes and increase autophagic flux. The observed molecular weight of TRAPPC12 is 98 kDa, which is consistent with what has been described in the literature (PMID: 28240221, PMID: 38439956).
实验方案
Product Specific Protocols | |
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WB protocol for TRAPPC12 antibody 24555-1-AP | Download protocol |
IP protocol for TRAPPC12 antibody 24555-1-AP | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |