Anti-ADA Antibody (CAB5151)
- SKU:
- CAB5151
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Cell Biology
Description
| 抗体名: | Anti-ADA Antibody |
| 抗体コード: | CAB5151 |
| 抗体サイズ: | 20uL, 50uL, 100uL |
| 申し込み: | WB |
| 反応性: | Human, Mouse |
| 宿主種: | Rabbit |
| 免疫原: | A synthesized peptide derived from human ADA |
| 申し込み: | WB |
| 推奨希釈: | WB 1:500 - 1:2000 |
| 反応性: | Human, Mouse |
| ポジティブサンプル: | Jurkat, Mouse stomach |
| 免疫原: | A synthesized peptide derived from human ADA |
| 精製方法: | Affinity purification |
| ストレージバッファ: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 0.05% BSA, 50% glycerol, pH7.3. |
| アイソタイプ: | IgG |
| 順序: | Email for sequence |
| 遺伝子ID: | 100 |
| Uniprot: | P00813 |
| セルラーロケーション: | |
| 計算された分子量: | 41kDa |
| 観察された分子量: | 45KDa |
| 同義語: | |
| バックグラウンド: | This gene encodes an enzyme that catalyzes the hydrolysis of adenosine to inosine. Various mutations have been described for this gene and have been linked to human diseases. Deficiency in this enzyme causes a form of severe combined immunodeficiency disease (SCID), in which there is dysfunction of both B and T lymphocytes with impaired cellular immunity and decreased production of immunoglobulins, whereas elevated levels of this enzyme have been associated with congenital hemolytic anemia. [provided by RefSeq, Jul 2008] |
| UniProt Protein Function: | ADA: a enzyme that converts adenosine + H2O into inosine + NH3. Found in all tissues, occurs in large amounts in T-lymphocytes and, at the time of weaning, in gastrointestinal tissues. Genetic ADA deficiencies are a cause of autosomal recessive severe combined immuno-deficiency (SCID). Hereditary hemolytic anemia is caused by expression levels in erythrocytes 50-70 times greater than the norm. |
| UniProt Protein Details: | Protein type:Hydrolase; Nucleotide Metabolism - purine; EC 3.5.4.4 Chromosomal Location of Human Ortholog: 20q13.12 Cellular Component: cell surface; cytoplasm; cytosol; external side of plasma membrane; lysosome; membrane; plasma membrane Molecular Function:adenosine deaminase activity; protein binding; zinc ion binding Biological Process: adenosine catabolic process; hypoxanthine salvage; inosine biosynthetic process; negative regulation of adenosine receptor signaling pathway; purine nucleotide salvage; purine salvage; regulation of cell-cell adhesion mediated by integrin; response to hypoxia; T cell activation Disease: Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-negative, B Cell-negative, Nk Cell-negative, Due To Adenosine Deaminase Deficiency |
| NCBI Summary: | This gene encodes an enzyme that catalyzes the hydrolysis of adenosine to inosine. Various mutations have been described for this gene and have been linked to human diseases. Deficiency in this enzyme causes a form of severe combined immunodeficiency disease (SCID), in which there is dysfunction of both B and T lymphocytes with impaired cellular immunity and decreased production of immunoglobulins, whereas elevated levels of this enzyme have been associated with congenital hemolytic anemia. [provided by RefSeq, Jul 2008] |
| UniProt Code: | P00813 |
| NCBI GenInfo Identifier: | 113339 |
| NCBI Gene ID: | 100 |
| NCBI Accession: | P00813.3 |
| UniProt Secondary Accession: | P00813,Q53F92, Q6LA59, |
| UniProt Related Accession: | P00813 |
| Molecular Weight: | 40,764 Da |
| NCBI Full Name: | Adenosine deaminase |
| NCBI Synonym Full Names: | adenosine deaminase |
| NCBI Official Symbol: | ADA |
| NCBI Protein Information: | adenosine deaminase |
| UniProt Protein Name: | Adenosine deaminase |
| UniProt Synonym Protein Names: | Adenosine aminohydrolase |
| Protein Family: | ADAM |
| UniProt Gene Name: | ADA |
| UniProt Entry Name: | ADA_HUMAN |
 | Western blot - ADA Rabbit mAb (CAB5151) |