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Details for Product No. ABIN396192

Oculocerebrorenal Syndrome of Lowe (OCRL) antibody

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Antigen
Synonyms INPP5F, LOCR, NPHL2, OCRL-1, OCRL1, BB143339, 9530014D17Rik, OCRL, wu:fi09g03, zgc:152864, locr, nphl2, ocrl1, inpp5f
Reactivity
»Alternatives Human
Host
»Alternatives Mouse
Clonality (Clone) Monoclonal ()
Conjugate
»Alternatives Un-conjugated
Application
»Alternatives ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)
Pubmed 5 references available
Catalog no. ABIN396192
Quantity 0.1 mg
Price
450.00 $   Plus shipping costs $45.00
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Availability Will be delivered in 2 to 3 Business Days
Immunogen OCRL (NP_000267, 146 a.a. ~ 240 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 K
Clone 4A6
Isotype IgG2a kappa
Specificity OCRL (NP_000267, 146 a.a. ~ 240 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Purification This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.
Alternative Name OCRL
Background Synonyms: Serine protease inhibitor J6, 47 kDa heat shock protein, Collagen-binding protein, Colligin, Serpin H1,Hsp47, Cbp1, Serpinh1
Molecular Weight 104205 DA
Gene ID 12406
UniProt NP_000267
Research Area Cell Structure
Application Notes ELISA ~~ 1ug/ml~3ng/ml Western blot ~~ 1:500~1000 Immunohistochemistry ~~ 1.5ug/ml
Comment

Background: This gene encodes a phosphatase enzyme that is involved in actin polymerization and is found in the trans-Golgi network. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease.

Restrictions For Research Use only
Buffer PBS with 0.09% (w/v) sodium azide.
Preservative Sodium azide
Storage 4 °C/-20 °C
Storage Comment Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles
Expiry Date 6 months
Background publications Tosetto, Addis, Caridi et al.: "Locus heterogeneity of Dent's disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations." in: Pediatric nephrology (Berlin, Germany), Vol. 24, Issue 10, pp. 1967-73, 2009 (PubMed).

Coon, Mukherjee, Hanna et al.: "Lowe syndrome patient fibroblasts display Ocrl1-specific cell migration defects that cannot be rescued by the homologous Inpp5b phosphatase." in: Human molecular genetics, Vol. 18, Issue 23, pp. 4478-91, 2009 (PubMed).

Cui, Guerriero, Szalinski et al.: "OCRL1 function in renal epithelial membrane traffic." in: American journal of physiology. Renal physiology, Vol. 298, Issue 2, pp. F335-45, 2010 (PubMed).

Coutton, Monnier, Rendu et al.: "Development of a multiplex ligation-dependent probe amplification (MLPA) assay for quantification of the OCRL1 gene." in: Clinical biochemistry, Vol. 43, Issue 6, pp. 609-14, 2010 (PubMed).

Swan, Tomasini, Pirruccello et al.: "Two closely related endocytic proteins that share a common OCRL-binding motif with APPL1." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 107, Issue 8, pp. 3511-6, 2010 (PubMed).

Alternatives for antigen "Oculocerebrorenal Syndrome of Lowe (OCRL)", type "Antibodies"
Hosts (31), (7)
Reactivities (38), (20), (14), (12), (12), (12)
Applications (27), (24), (10), (9), (6), (3), (1), (1), (1), (1)
Conjugates (1), (1), (1), (1), (1), (1), (1), (1), (1), (1), (1)
Epitopes (7), (4), (3), (3), (1), (1), (1), (1), (1)
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