PASD1 antibodies are designed to detect the PASD1 protein, which is primarily expressed in germ cells but aberrantly upregulated in various cancers. These antibodies enable the identification of PASD1 expression patterns in tissues and cells, aiding in cancer diagnosis, immunotherapy research, and circadian rhythm studies.
Target: PASD1 protein (isoforms PASD1-1 and PASD1-2).
Antigen Specificity:
PASD1a: Binds to the N-terminal region shared by both PASD1-1 and PASD1-2.
PASD1b: Targets the unique C-terminal region of PASD1-2.
Applications: Immunohistochemistry (IHC), Western blot (WB), ELISpot assays, and cytotoxicity studies .
PASD1 has two splice variants:
| Isoform | Size | Expression | Antibody Target |
|---|---|---|---|
| PASD1-1 | 639 aa | Common region | PASD1a |
| PASD1-2 | 773 aa | Unique C-terminus | PASD1b |
PASD1a detects both isoforms, while PASD1b is specific to PASD1-2.
PASD1-2 is more frequently expressed in colorectal cancer (CRC) and polyps compared to PASD1-1 .
PASD1 antibodies are critical for studying cancer biology and immune responses.
Used to assess PASD1 protein localization in tissues.
PASD1 expression is detected in 31.7% of CRC and 29.4% of polyps samples .
In melanoma, PASD1 is expressed in skin tumors but not ovarian cancers .
Validates PASD1 protein presence in cell lines.
| Cell Line | PASD1 Detection | Source |
|---|---|---|
| SW480 (CRC) | Strong signal (72–87 kDa) | Proteintech Antibody (12976-1-AP) . |
| HCT116 (CRC) | No detection | Negative control . |
PASD1 peptides induce CD4+ T-cell responses in cancer patients.
| Cancer Type | Immunogenic Peptides | Patient Response Rate |
|---|---|---|
| DLBCL | PASD1(6), PASD1(7) | 14/32 patients |
| CRC/Polyps | PASD1(1), PASD1(3) | 21.7% (CRC), 23.5% (polyps) |
Circadian Rhythm Modulation: PASD1 suppresses CLOCK:BMAL1 activity, offering insights into cancer-related circadian disruption .
Immunotherapy: PASD1-specific CD4+ T-cell responses are candidates for peptide-based vaccines in DLBCL and CRC .
Biomarker: PASD1 expression correlates with advanced-stage CRC and rectosigmoid tumors .