Sequestosome 1 Phospho-Thr269/Ser272 (SQSTM1 pT269/pS272) Antibody
572€ (100 µl)
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935106861
info@markelab.com
name
Sequestosome 1 Phospho-Thr269/Ser272 (SQSTM1 pT269/pS272) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx412199
tested applications
WB
Description
Sequestosome 1 Phospho-Thr269/Ser272 (SQSTM1 pT269/pS272) Antibody is a Rabbit Polyclonal antibody against p62 (pThr269/pSer272). This antibody detects p62 phosphorylated at residue(s) Thr269/Ser272.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Sequestosome 1 Phospho-Thr269/Ser272 (SQSTM1 pT269/pS272) |
| Host | Rabbit |
| Reactivity | Human |
| Assay Data | Modification: Phosphorylation // Target Modification: Thr269/Ser272 |
| Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Purified |
| Size 1 | 100 µl |
| Form | Liquid |
| Tested Applications | WB |
| Buffer | HEPES buffered saline, 1% BSA. Contains sodium azide and glycerol. |
| Availability | Shipped within 3-7 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | Q13501 |
| Alias | SQSTM1, A170, OSIL, PDB3, ZIP3, p60, p62, p62B, FTDALS3, NADGP, DMRV |
| Background | Antibody anti-SQSTM1 |
| Status | RUO |
Descripción
SQSTM1, also known as p62, is an adaptor protein involved in selective autophagy, protein degradation, and cellular stress responses. It acts as a scaffold protein that interacts with ubiquitinated proteins and autophagy-related proteins like LC3, facilitating the delivery of misfolded or damaged proteins to the autophagosome for degradation. SQSTM1 also functions in signaling pathways such as NF-κB activation, oxidative stress responses, and mTOR signaling, where it regulates inflammation, apoptosis, and metabolism. It is highly expressed in various tissues and is essential for maintaining protein homeostasis under stress conditions. Dysregulation or mutations in SQSTM1 are associated with neurodegenerative diseases like ALS and Parkinson’s disease, Paget's disease of bone, and cancer due to impaired autophagy and accumulation of protein aggregates. Knockout studies reveal defects in autophagic flux, increased oxidative stress, and disrupted cellular homeostasis, underscoring its central role in protein quality control and cellular stress adaptation.
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