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| 产品: | C-MYC-tag 抗体 |
| 货号: | T0052 |
| 描述: | Rabbit polyclonal antibody to C-MYC-tag |
| 应用: | WB IF/ICC |
| 反应: | All |
| 蛋白号: | |
| RRID: | AB_2843446 |
产品描述
来源:
Rabbit
应用:
WB 1:3000-1:10000, IF/ICC: 1:200
*The optimal dilutions should be determined by the end user.
*Tips:
*The optimal dilutions should be determined by the end user.
*Tips:
WB: 适用于变性蛋白样本的免疫印迹检测. IHC: 适用于组织样本的石蜡(IHC-p)或冰冻(IHC-f)切片样本的免疫组化/荧光检测. IF/ICC: 适用于细胞样本的荧光检测. ELISA(peptide): 适用于抗原肽的ELISA检测.
反应:
All
克隆:
Polyclonal
特异性:
The C-Myc tag antibody can detect C-Myc fusion proteins.
RRID:
AB_2843446
引用格式: Affinity Biosciences Cat# T0052, RRID:AB_2843446.
引用格式: Affinity Biosciences Cat# T0052, RRID:AB_2843446.
偶联:
Unconjugated.
纯化:
Affinity-chromatography.
保存:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
别名:
展开/折叠
C-MYC-tag;CMYC;myc;
抗原和靶标
免疫原:
A synthetic peptide EQKLISEEDL coupled to KLH.
描述:
c-Myc-tag antibody is part of the Tag series of antibodies, the best quality in the research. The immunogen of c-Myc tag antibody is a synthetic peptide corresponding to residues 410-419 of the human p62 c-myc protein conjugated to KLH. C-Myc tag antibody is suitable for detecting the expression level of c-Myc or its fusion proteins where the c-Myc tag is terminal or internal.
文献引用
1). Paraquat is an agonist of STIM1 and increases intracellular calcium levels. Communications Biology
(PubMed: 36310238)
[IF=5.9]
2). Chicken bromodomain-containing protein 2 interacts with the Newcastle disease virus matrix protein and promotes viral replication. Veterinary Research
(PubMed: 32962745)
[IF=4.4]
Application: WB Species: Chicken Sample: DF-1 cells
Figure 3 |Conservation analysis of the BRD2/ET domain from diferent species.C Identifcation of the interaction between the chBRD2/ET or huBRD2/ET domain and NDV M protein. Upper panel, schematic representation of the chBRD2/ET domain and huBRD2/ET domain. Lower panel,the combined plasmids were co-transfected into DF-1 cells, and 36 h after transfection, the interaction between HA-M and Myc-chBRD2/ET or Myc-huBRD2/ET was identifed by co-IP assay.
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