MULTI SCIENCES
RUO Human CarBonic Anhydrase XII/CA12 ELISA Kit
RUO Human CarBonic Anhydrase XII/CA12 ELISA Kit
SKU:EK1245
Product Details
| Brand | MultiSciences |
|---|---|
| CatNum | 70-EK1245 |
| Product Name | Human Carbonic Anhydrase XII/CA12 ELISA Kit |
| Customs Name | Human Carbonic Anhydrase XII/CA12 ELISA Kit |
| Application | ELISA |
| Reactivity | Human |
| Assay Type | Sandwich ELISA |
| Suitable Sample Type | serum, plasma, cell culture supernates |
| Format | 96-well strip plate |
| Storage | 4℃ (unopened) standard stored at -20℃, others stored at 4℃ (opened) |
| Shipping Condition | 4℃ |
| Sample Volume | 50 μl |
| Sensitivity | 1.72 pg/ml |
| Standard Curve Range | 78.13 - 5000 pg/ml |
| Spike Recovery Range | 79 % - 109 % |
| Mean Spike Recovery | 0.93 |
| CV of Intra plate | 2.1 % - 2.3 % |
| CV of Inter plate | 2.1 % - 3.7 % |
| Components | 96-well polystyrene microplate coated with a monoclonal antibody against CA12 Human CA12 Standard, lyophilized CA12 Detect Antibody Standard Diluent Assay Buffer (10×) Substrate (TMB) Stop Solution Washing Buffer (20×) Plate Covers |
| Describtion | This assay employs the quantitative sandwich enzyme immunoassay technique for the quantitative detection of human CA12. The Human Carbonic Anhydrase XII/CA12 ELISA is for research use only. Not for diagnostic or therapeutic procedures. Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. Carbonic anhydrase XII (CA12) is a type I membrane protein that is highly expressed in normal tissues, such as kidney, colon and pancreas, and has been found to be overexpressed in 10% of clear cell renal carcinomas. Two transcript variants encoding different isoforms have been identified for this gene. Mutations in the gene encoding CA12 have been shown to be associated with an autosomal recessive form of hyponatremia due to salt wasting in sweat. |
