Date published: 2026-8-18

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SQSTM1/p62 Antibody (D-3): sc-28359

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Datasheets
  • SQSTM1/p62 Antibody (D-3) is a mouse monoclonal IgG1 κ SQSTM1/p62 antibody, cited in 614 publications, provided at 200 µg/ml
  • raised against amino acids 151-440 of SQSTM1 of human origin
  • SQSTM1/p62 Antibody (D-3) is recommended for detection of SQSTM1 of human origin by WB, IP, IF, IHC(P) and ELISA
  • Anti-SQSTM1/p62 Antibody (D-3) is available conjugated to agarose for IP; HRP for WB, IHC(P) and ELISA; and to either phycoerythrin or FITC for IF, IHC(P) and FCM
  • also available conjugated to Alexa Fluor® 488, Alexa Fluor® 546, Alexa Fluor® 594 or Alexa Fluor® 647 for WB (RGB), IF, IHC(P) and FCM, and for use with RGB fluorescent imaging systems, such as iBright™ FL1000, FluorChem™, Typhoon, Azure and other comparable systems
  • also available conjugated to Alexa Fluor® 680 or Alexa Fluor® 790 for WB (NIR), IF and FCM; for use with Near-Infrared (NIR) detection systems, such as LI-COR®Odyssey®, iBright™ FL1000, FluorChem™, Typhoon, Azure and other comparable systems
  • m-IgG Fc BP-HRP is the preferred secondary detection reagent for SQSTM1/p62 Antibody (D-3) for WB and IHC(P) applications. This reagent is now offered in a bundle with SQSTM1/p62 Antibody (D-3) (see ordering information below).
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SQSTM1 Antibody (D-3) is a mouse monoclonal IgG1 kappa light chain antibody specifically designed to detect human SQSTM1 protein, also known as p62, across applications including western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), immunohistochemistry with paraffin-embedded sections (IHCP), and enzyme-linked immunosorbent assay (ELISA). SQSTM1 monoclonal antibody (D-3) targets the amino acid region 151-440 of human SQSTM1 protein, ensuring precise binding and reliable detection. SQSTM1, also called p60, p62, A170, DMRV, OSIL, PDB3, ZIP3, p62B, EBIAP, NADGP, and FTDALS3, plays a critical role in cellular processes such as autophagy, where SQSTM1 acts as a selective autophagy receptor by recognizing and binding to ubiquitinated proteins, facilitating their degradation. Post-translational modifications of SQSTM1, including phosphorylation and ubiquitination, are essential for regulating protein homeostasis and signaling pathways. Phosphorylation of SQSTM1 enhances binding to ubiquitinated targets and autophagic machinery, promoting efficient autophagic flux and preventing protein aggregate accumulation that can lead to cellular dysfunction. Anti-SQSTM1 antibody (D-3) is available in both non-conjugated and various conjugated forms, such as agarose, horseradish peroxidase (HRP), phycoerythrin (PE), fluorescein isothiocyanate (FITC), and multiple Alexa Fluor® conjugates, providing flexibility for diverse experimental setups. SQSTM1 (D-3) antibody is particularly valuable in studying diseases like Paget′s disease of bone, where mutations in the ubiquitin-associated (UBA) domain of SQSTM1 disrupt normal function in aggregate sequestration and cell survival, leading to increased bone resorption and abnormal bone formation. Anti-SQSTM1 antibody (D-3) helps researchers gain deeper insights into molecular mechanisms underlying such conditions, facilitating targeted therapy development and improving understanding of SQSTM1′s role in cellular homeostasis and disease pathology.

For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA

LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences

SQSTM1/p62 Antibody (D-3) References:

  1. Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease.  |  Hocking, LJ., et al. 2002. Hum Mol Genet. 11: 2735-9. PMID: 12374763
  2. Structure of the ubiquitin-associated domain of p62 (SQSTM1) and implications for mutations that cause Paget's disease of bone.  |  Ciani, B., et al. 2003. J Biol Chem. 278: 37409-12. PMID: 12857745
  3. Three novel mutations in SQSTM1 identified in familial Paget's disease of bone.  |  Johnson-Pais, TL., et al. 2003. J Bone Miner Res. 18: 1748-53. PMID: 14584883
  4. Paget's disease of bone.  |  Rousière, M., et al. 2003. Best Pract Res Clin Rheumatol. 17: 1019-41. PMID: 15123049
  5. Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees.  |  Good, DA., et al. 2004. Bone. 35: 277-82. PMID: 15207768
  6. Sequestosome 1/p62 is a polyubiquitin chain binding protein involved in ubiquitin proteasome degradation.  |  Seibenhener, ML., et al. 2004. Mol Cell Biol. 24: 8055-68. PMID: 15340068
  7. Etiology of Paget's disease and osteoclast abnormalities.  |  Reddy, SV. 2004. J Cell Biochem. 93: 688-96. PMID: 15389972
  8. Structural and functional studies of mutations affecting the UBA domain of SQSTM1 (p62) which cause Paget's disease of bone.  |  Layfield, R., et al. 2004. Biochem Soc Trans. 32: 728-30. PMID: 15493999
  9. Ubiquitin-associated domain mutations of SQSTM1 in Paget's disease of bone: evidence for a founder effect in patients of British descent.  |  Lucas, GJ., et al. 2005. J Bone Miner Res. 20: 227-31. PMID: 15647816

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

SQSTM1/p62 Antibody (D-3)

sc-28359
200 µg/ml
$322.00

SQSTM1/p62 Antibody (D-3): m-IgG Fc BP-HRP Bundle

sc-525526
200 µg Ab; 10 µg BP
$361.00

SQSTM1/p62 Antibody (D-3) AC

sc-28359 AC
500 µg/ml, 25% agarose
$424.00

SQSTM1/p62 Antibody (D-3) HRP

sc-28359 HRP
200 µg/ml
$322.00

SQSTM1/p62 Antibody (D-3) FITC

sc-28359 FITC
200 µg/ml
$336.00

SQSTM1/p62 Antibody (D-3) PE

sc-28359 PE
200 µg/ml
$349.00

SQSTM1/p62 Antibody (D-3) Alexa Fluor® 488

sc-28359 AF488
200 µg/ml
$364.00

SQSTM1/p62 Antibody (D-3) Alexa Fluor® 546

sc-28359 AF546
200 µg/ml
$364.00

SQSTM1/p62 Antibody (D-3) Alexa Fluor® 594

sc-28359 AF594
200 µg/ml
$364.00

SQSTM1/p62 Antibody (D-3) Alexa Fluor® 647

sc-28359 AF647
200 µg/ml
$364.00

SQSTM1/p62 Antibody (D-3) Alexa Fluor® 680

sc-28359 AF680
200 µg/ml
$364.00

SQSTM1/p62 Antibody (D-3) Alexa Fluor® 790

sc-28359 AF790
200 µg/ml
$364.00