PTGX-AID-2E11
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Brand | ProteoGenix |
Product type | Primary antibodies |
Reactivity | Human, Mouse |
Clonality | Monoclonal |
Host species | Mouse |
Applications | E, WB, IC,IP |
Brand: | ProteoGenix |
Proteogenix reference: | PTGX-AID-2E11 |
Product type: | Primary antibodies |
Clonality: | Monoclonal |
Product name: | Mouse Monoclonal antibody to human AID (Activation induced cytidine deaminase) |
Host species: | Mouse |
Target species: | Human |
Reactivity: | Human, Mouse |
Applications: | E, WB, IC,IP |
Size: | 100µl |
Clone name: | 1AIDâ2E11 |
Uniprot: | #N/A |
Immunogen: | Synthetic peptide coupled to Ovalbumin: (C)-EVDDLRDAFRMLGF corresponding to aa 185 to 198 of mouse AID. |
Specificity: | mouse and human AID |
Dilution: | 1/500 â 1/5000 |
Alternative names: | Anti-AICDA antibody, Activation induced cytidine deaminase antibody, Activation induced deaminase antibody, Activation-induced cytidine deaminase antibody, AICDA antibody, AICDA_HUMAN antibody, AID antibody, ARP 2 antibody, ARP2 antibody, CDA 2 antibody, CDA2 antibody, Cytidine aminohydrolase antibody, HIGM2 antibody, Integrated into Burkitt's lymphoma cell line Ramos antibody |
Isotype: | IgG1, k |
Form: | liquid/frozen |
Spec:conjugate/tag/label: | Unconjugated |
Research area: | DNA Damage and Repair, Epigenetics & Nuclear Signalling, Immunology |
Background information: | Mouse monoclonal anti-AID (Activation-induced cytidine deaminase), clone 1AID-2E11 recognizes mouse and human AID, encoded by the AICDA (Activation-induced cytidine deaminase) gene. AICDA was originally discovered as a homolog of the apolipoprotein B RNA-editing cytidine deaminase 1 (APOBEC1) that presented cytidine deaminase properties in stimulated B cell lines. AICDA is essential for somatic hypermutation and class switch recombination in B cells, but inappropriate or dysregulated expression AID is usually found in tumors and B cell neoplasms. This gene encodes a RNA-editing deaminase that is a member of the cytidine deaminase family. The protein is implicated in somatic hypermutation, gene conversion, and class-switch recombination of immunoglobulin genes. Deficiencies in this gene are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2). |
Publications: | / |
Storage: | Store at -20°C. Aliquot to avoid repeated freezing and thawing. |
Delivery lead time in business days in europe: | 2-3 |
Delivery conditions: | Dry Ice |
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