Bs-9005R-Cy7 [Conjugated Primary Antibody]

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bs-9005R-Cy7 [Conjugated Primary Antibody] Rabbit Anti-CECR1 Polyclonal Antibody, Cy7 Conjugated www.biossusa.com [email protected] 800.501.7654 [DOMESTIC] +1.781.569.5821 [INTERNATIONAL] D A T A S H E E T Host: Rabbit Conjugation: Cy7 Target Protein: CECR1 Excitation/ 743nm/767nm Emission: Clonality: Polyclonal Isotype: IgG Size: 100ul Entrez Gene: 51816 Concentration: 1ug/ul Swiss Prot: Applications: IF(IHC-P)(1:50-200) Source: KLH conjugated synthetic peptide derived from human CECR1/ADGF Cross Reactive Human Species: Purification: Purified by Protein A. Caution: For research use only. Not for human or animal Storage: Aqueous buffered solution containing 100ug/ml BSA, 50% glycerol and 0.09% sodium azide. therapeutic or diagnostic use. Store at 4°C for 12 months. Background: CECR1 is a member of the adenosine and AMP deaminases family. It may act as a growth factor and have adenosine deaminase activity. It is a candidate gene for cat eye syndrome. Two transcript variants encoding distinct isoforms have been identified for this gene.Adenosine deaminase is an enzyme that is present in most tissues and exists predominantly as a monomer, although in some tissues it is associated with adenosine deaminase-binding protein. Adenosine deaminase degrades extracellular adenosine, which is toxic for lymphocytes. A novel family of growth factors that share sequence similarity to adenosine deaminase has been identified. The cat eye syndrome critical region protein (CECR) family includes CECR1, CECR2, CECR3, CECR4, CECR5, CECR6, CECR7, CECR8 and CECR9. The genes encoding CECR proteins are candidates for Cat Eye Syndrome (CES), a developmental disorder associated with the duplication of a 2 Mb region of 22q11.2. CES is characterized by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. CECR family members are widely expressed. Specifically, CECR1 has the highest expression in adult heart, lung, lymphoblasts and placenta. CECR2 is also involved in neurulation and chromatin remodeling. Mutations in the CECR2 gene result in neural tube defects. .

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Role of RUNX1 in Aberrant Retinal Angiogenesis Jonathan D
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