WB result of ZBTB21 Recombinant Rabbit mAb
Primary antibody: ZBTB21 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: BxPC-3 whole cell lysate 20 µg
Lane 2: RPMI-8226 whole cell lysate 20 µg
Lane 3: 293T whole cell lysate 20 µg
Negative control: BxPC-3 whole cell lysate
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 119 kDa
Observed MW: 110 kDa
This blot was developed with high sensitivity substrate
Product Details
Product Details
Product Specification
| Host | Rabbit |
| Antigen | ZBTB21 |
| Synonyms | Zinc finger and BTB domain-containing protein 21; KIAA1227; ZNF295 |
| Location | Nucleus |
| Accession | Q9ULJ3 |
| Clone Number | S-3936-49 |
| Antibody Type | Recombinant mAb |
| Isotype | IgG |
| Application | WB |
| Reactivity | Hu |
| Positive Sample | RPMI-8226, 293T |
| Purification | Protein A |
| Concentration | 2 mg/ml |
| Conjugation | Unconjugated |
| Physical Appearance | Liquid |
| Storage Buffer | PBS, 40% Glycerol, 0.05% BSA, 0.02% sodium azide |
| Stability & Storage | 12 months from date of receipt / reconstitution, -20 °C as supplied |
Dilution
| application | dilution | species |
| WB | 1:500-1:1000 | Hu |
Background
ZBTB21 (Zinc Finger and BTB Domain-Containing Protein 21, also known as ZNF295) is a ubiquitously expressed transcriptional repressor in humans. Its protein structure features an N-terminal BTB/POZ domain, which mediates protein dimerization and interactions with transcriptional co-repressor complexes, as well as multiple C2H2-type zinc finger domains responsible for sequence-specific DNA binding. As a critical node in epigenetic regulation, ZBTB21 restricts STAT1-mediated chromatin accessibility by reducing H3K27ac histone modifications, thereby epigenetically silencing GSDMD-dependent pyroptosis. Simultaneously, it suppresses tumor cell surface MHC-I antigen presentation by attenuating IRF1 expression and its transcriptional activation capacity. This dual inhibitory mechanism makes ZBTB21 a major driver of tumor immune evasion. Notably, recent studies have demonstrated that pharmacological inhibition of ZBTB21 with dobutamine or genetic knockout of ZBTB21 can simultaneously relieve the suppression of both pyroptosis and antigen presentation, significantly enhancing CD8⁺ T cell anti-tumor immune responses and exhibiting synergistic effects with anti-PD-1 immunotherapy, positioning ZBTB21 as a promising novel therapeutic target for cancer treatment.
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Picture
Western Blot
