Product Name :
Rabbit anti Human SPARC
Description :
| Isotype IgG | Product Type Polyclonal Antibody | Units 100 µg | Host Rabbit | Species Reactivity Human SPARC may cross react with SPARCL1 | Application ELISA Immunohistochemistry Western Blotting
Background :
Rabbit immunized with a synthetic peptide derived from the human SPARC protein.
Source :
SPARC is a key factor in cell-matrix interactions and possibly tumour aggressiveness. The SPARC gene, which encodes a multifunctional glycoprotein with roles in tissue development, remodelling and fibrosis. A regulator of cell-extracellular matrix (ECM) interactions, SPARC represents a major factor in the ECM remodelling occurring during tumour invasion. in silico analysis reveals 4 UTR-SNPs located in the 3 -UTR of the SPARC gene, corresponding to 1474 g a, 1551 g c, 1922 t g and 2072 c t changes, which are significantly associated with tumoral state of the tissue. Of all hits, the 2072 SPARC polymorphism had the best association with cancer. SPARC therefore is a gene involved in a number of diseases including rheumatoid arthritis, scleroderma, tumor development and metastasis. SPARC variants have been detected in tumour samples of patients with acute myeloblastic leukemia (AML). Synonyms: Secreted Protein Acidic and Rich in Cysteine, SPARC, SPARC-related modular calcium-binding protein 2 [Precursor], Secreted modular calcium-binding protein 2, SMOC-2, Smooth muscle-associated protein 2, SMAP-2 <
Product :
Product Form: Unconjugated Formulation: Provided as solution in phosphate buffered saline with 0.08% sodium azide Purification Method: Ammonium Sulfate Precipitation Concentration: See vial for concentration
Specificity :
Applications :
Antibody can be used for Western blotting (1-5 µg/ml), Immunohistochemistry and ELISA. Optimal concentration should be evaluated by serial dilutions. Functional Analysis: Western Blotting, Immunohistochemistry. Positive Control: Antibody tested on mouse heart lysate
Storage :
Product should be stored at -20°C. Aliquot to avoid freeze/thaw cycles Product Stability: See expiration date on vial Shipping Conditions: Ship at ambient temperature, freeze upon arrival
Caution :
This product is intended FOR RESEARCH USE ONLY, and FOR TESTS IN VITRO, not for use in diagnostic or therapeutic procedures involving humans or animals. It may contain hazardous ingredients. Please refer to the Safety Data Sheets (SDS) for additional information and proper handling procedures. Dispose product remainders according to local regulations.This datasheet is as accurate as reasonably achievable, but our company accepts no liability for any inaccuracies or omissions in this information.
References :
1. Shi Q, et al. ‘Targeting SPARC expression decreases glioma cellular survival and invasion associated with reduced activities of FAK and ILK kinases.’ Oncogene. 2007 Jan 8; [Epub ahead of print] PMID: 17213807 2. Aouacheria A, et al. ‘In silico whole-genome screening for cancer-related single-nucleotide polymorphisms located in human mRNA untranslated regions.’ BMC Genomics. 2007 Jan 3;8(1):2 [Epub ahead of print] PMID: 17201911 3. Xue LY, et al. ‘Tissue microarray analysis reveals a tight correlation between protein expression pattern and progression of esophageal squamous cell carcinoma.’BMC Cancer. 2006 Dec 22;6(1):296 [Epub ahead of print] PMID: 17187659 4. Arp HP, et al. ‘Predicting the partitioning behavior of various highly fluorinated compounds.’ Environ Sci Technol. 2006 Dec 1;40(23):7298-304. PMID: 17180981 5. Kelly KA, et al. ‘SPARC is a VCAM-1 counter-ligand that mediates leukocyte transmigration.’ J Leukoc Biol. 2007, March 81(3); 748-56. 6. Markovic, S., et al. ‘Tumor SPARC microenvironment signature (SMS) and plasma levels in a phase II trial of unresectable stage IV melanoma treated with nab-paclitaxel and carboplatin: A translational study of NCCTG trial N057E.’ J. Clin. Oncol. 2010, Vol. 28, No. 15, 8578 7. Weiss, G.J., et al. ‘Molecular characterization of interdigitating dendritic cell sarcoma.’ Rare Tumors, 2010, 2:e50 8. Alonso, E.N., et al. ‘Genes Related to Suppression of Malignant Phenotype Induced by Maitake D-Fraction in Breast Cancer Cells.’ J. Med. Food., 16, 602-617 (2013).
Related websites: https://www.medchemexpress.com/antibodies.html
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