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Description
GSDMD Recombinant Rabbit mAb (S-3035)Product Specification Host Rabbit Antigen GSDMD Synonyms Gasdermin D; Gasdermin domain containing protein 1; DFNA5L; GSDMDC1 Location Cytoplasm, Cell membrane Accession P57764 Clone Number S 3035 Antibody Type Recombinant mAb Isotype IgG Application WB Reactivity Hu Positive Sample PC 3, A431, Jurkat Purification Protein A Concentration 0. 5 mg ml Conjugation Unconjugated Physical Appearance Liquid Storage Buffer PBS, 40% Glycerol, 0. 05% BSA, 0. 03%
Product Specification
| Host | Rabbit |
| Antigen | GSDMD |
| Synonyms | Gasdermin-D; Gasdermin domain-containing protein 1; DFNA5L; GSDMDC1 |
| Location | Cytoplasm, Cell membrane |
| Accession | P57764 |
| Clone Number | S-3035 |
| Antibody Type | Recombinant mAb |
| Isotype | IgG |
| Application | WB |
| Reactivity | Hu |
| Positive Sample | PC-3, A431, Jurkat |
| Purification | Protein A |
| Concentration | 0.5 mg/ml |
| Conjugation | Unconjugated |
| Physical Appearance | Liquid |
| Storage Buffer | PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300 |
| Stability & Storage | 12 months from date of receipt / reconstitution, -20°C as supplied |
Dilution
| application | dilution | species |
| WB | 1:1000 | Hu |
Background
Gasdermin D (GSDMD) is a crucial protein within the gasdermin family, playing a key role in executing pyroptosis, a form of lytic, inflammatory cell death. The full-length GSDMD protein is inactive and consists of a 31 kD N-terminal pore-forming domain and a 22 kD C-terminal suppression domain. Upon activation by caspases such as caspase-1, -4, -5, or -11, the interdomain linker is cleaved, releasing the N-terminal fragment (GSDMD-NT) from the inhibitory C-terminal domain. The freed GSDMD-NT translocates to the plasma membrane, oligomerizes, and forms pores with an inner diameter of approximately 10–14 nm, leading to cell lysis, cytokine release (such as IL-1β and IL-18), and disruption of ion and water balance. This pore formation is a critical step in mediating inflammation and immune responses. GSDMD is also implicated in various diseases, including sepsis, myocardial ischemia/reperfusion injury, and certain cancers. Research on selective GSDMD inhibitors is ongoing, aiming to block pyroptosis and reduce inflammation in pathological conditions.
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