Sequestosome 1 (SQSTM1) (AA 300-360) antibody

Details for Product No. ABIN350829
Request Want additional data for this product?

The Independent Validation Initiative strives to provide you with high quality data. Find out more

Antigen
Synonyms SQSTM1, sqstm1, MGC79491, A170, OSIL, PDB3, ZIP3, p60, p62, p62B, OSF-6, Osi, STAP, ZIP, sb:cb621, zgc:85784
Epitope
AA 300-360
(24), (16), (9), (9), (7), (7), (6), (6), (5), (5), (5), (4), (3), (3), (2), (2), (1), (1), (1), (1), (1), (1), (1), (1)
Reactivity
Human
(110), (30), (29), (14), (12), (12), (1), (1)
Host
Sheep
(91), (14), (4), (2)
Clonality
Polyclonal
Conjugate
Un-conjugated
(6), (6), (5), (4), (4), (4), (3), (3), (3), (1), (1), (1), (1), (1), (1), (1), (1)
Application
Immunohistochemistry (Frozen Paraffin-embedded Sections) (IHC (frpe)), Western Blotting (WB)
(83), (41), (31), (25), (24), (18), (18), (10), (7), (5), (3), (3), (3), (1)
Pubmed 10 references available
Quantity 500 µg
Options
Shipping to United States (Change)
Availability Will be delivered in 7 to 8 Business Days
Request Want additional data for this product?

The Independent Validation Initiative strives to provide you with high quality data. Find out more

Catalog No. ABIN350829
454.67 $
Plus shipping costs $45.00

Order hotline:

  • +1 404 474 4654
  • +1 888 205 9894 (TF)
Immunogen A synthetic peptide from aa region 300-360 of human SQSTM1 has been used as the antigen.
Isotype IgG
Specificity Specific for sequestosome-1.
Alternative Name SQSTM1
Background Function: Adapter protein which binds ubiquitin and may regulate the activation of NFKB1 by TNF-alpha, nerve growth factor (NGF) and interleukin-1. May play a role in titin/TTN downstream signaling in muscle cells. May regulate signaling cascades through ubiquitination. May be involved in cell differentiation, apoptosis, immune response and regulation of K(+) channels.
Subcellular location: Cytoplasm. Late endosome. Nucleus. Note=Sarcomere. In cardiac muscles localizes to the sarcomeric band. Localizes to late endosomes. May also localize to the nucleus. Accumulates in neurofibrillary tangles and in Lewy bodies of neurons from individuals with Alzheimer and Parkinson disease respectively. Enriched in Rosenthal fibers of pilocytic astrocytoma. In liver cells, accumulates in Mallory bodies associated with alcoholic hepatitis, Wilson disease, indian childhood cirrhosis and in hyaline bodies associated with hepatocellular carcinoma.
Tissue specificity: Ubiquitously expressed. Also known as: Sequestosome 1, phosphotyrosine-independent ligand for the Lck SH2 domain of 62 kDa, ubiquitin-binding protein p62, EBI3-associated protein of 60 kDa, p60, EBIAP, SQSTM1, A170, OSIL, PDB3, ZIP3, p62B.
Application Notes Use at a concentration of 10-50 µg/ml.
The optimal concentration should be determined by the end user.
Restrictions For Research Use only
Format Lyophilized
Reconstitution Reconstitute in 100 µL of sterile water. Centrifuge to remove any insoluble material.
Handling Advice Avoid freeze and thaw cycles.
Storage 4 °C/-20 °C
Storage Comment Maintain the lyophilised/reconstituted antibodies frozen at -20°C for long term storage and refrigerated at 2-8°C for a shorter term. When reconstituting, glycerol (1:1) may be added for an additional stability. Avoid freeze and thaw cycles.
Expiry Date 12 months
General Devergne, Hummel, Koeppen et al.: "A novel interleukin-12 p40-related protein induced by latent Epstein-Barr virus infection in B lymphocytes." in: Journal of virology, Vol. 70, Issue 2, pp. 1143-53, 1996 (PubMed).

Joung, Strominger, Shin: "Molecular cloning of a phosphotyrosine-independent ligand of the p56lck SH2 domain." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 93, Issue 12, pp. 5991-5, 1996 (PubMed).

Vadlamudi, Joung, Strominger et al.: "p62, a phosphotyrosine-independent ligand of the SH2 domain of p56lck, belongs to a new class of ubiquitin-binding proteins." in: The Journal of biological chemistry, Vol. 271, Issue 34, pp. 20235-7, 1996 (PubMed).

Stumptner, Heid, Fuchsbichler et al.: "Analysis of intracytoplasmic hyaline bodies in a hepatocellular carcinoma. Demonstration of p62 as major constituent." in: The American journal of pathology, Vol. 154, Issue 6, pp. 1701-10, 1999 (PubMed).

Hocking, Lucas, Daroszewska et al.: "Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease." in: Human molecular genetics, Vol. 11, Issue 22, pp. 2735-9, 2002 (PubMed).

Ciani, Layfield, Cavey et al.: "Structure of the ubiquitin-associated domain of p62 (SQSTM1) and implications for mutations that cause Paget's disease of bone." in: The Journal of biological chemistry, Vol. 278, Issue 39, pp. 37409-12, 2003 (PubMed).

Hocking, Lucas, Daroszewska et al.: "Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: genotype phenotype correlation, functional analysis, and structural consequences." in: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, Vol. 19, Issue 7, pp. 1122-7, 2004 (PubMed).

Good, Busfield, Fletcher et al.: "Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees." in: Bone, Vol. 35, Issue 1, pp. 277-82, 2004 (PubMed).

Nousiainen, Silljé, Sauer et al.: "Phosphoproteome analysis of the human mitotic spindle." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 103, Issue 14, pp. 5391-6, 2006 (PubMed).

Olsen, Blagoev, Gnad et al.: "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks." in: Cell, Vol. 127, Issue 3, pp. 635-48, 2006 (PubMed).

Validation Images
Did you look for something else?
back to top