Apolipoprotein E (APOE) (Isoform E3) Rabbit Polyclonal Antibody
CAT#: AP01142PU-S
Apolipoprotein E (APOE) (Isoform E3) rabbit polyclonal antibody, Aff - Purified
Size: 100 ug
Conjugation: Biotin
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CNY 3,910.00
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Specifications
Product Data | |
Applications | ELISA, WB |
Recommend Dilution | Indirect ELISA: To detect hApoE3 (using 100 μl/well antibody solution) a concentration of 0.5 - 2.0 μg/ml of this antibody is required. In conjunction with compatible secondary reagents, it allows the detection of at least 0.2 - 0.4 ng/well of recombinant hApoE3. Sandwich ELISA: To detect hApoE3 (using 100 μl/well antibody solution) a concentration of 0.5 - 2.0 μg/ml of this antibody is required. In conjunction with Biotinylated Anti-Human ApoE3 as a detection antibody, it allows the detection of at least 0.2 - 0.4 ng/well of recombinant hApoE3. Western blot: To detect hApoE3 this antibody can be used at a concentration of 0.1 - 0.2 µg/ml. Used in conjunction with compatible secondary reagents the detection limit for recombinant hApoE3 is 1.5 - 3.0 ng/lane, under either reducing or non-reducing conditions. |
Reactivity | Human |
Host | Rabbit |
Clonality | Polyclonal |
Immunogen | Highly pure (> 98%) E.coli derived, 34.4 kDa recombinant human ApoE3 |
Specificity | This antibody detects ApoE3. |
Formulation | PBS, pH 7.2 without preservatives. State: Aff - Purified State: Sterile filtered lyophilized Ig fraction |
Reconstitution Method | Restore in sterile water to a concentration of 0.1 - 1.0 mg/ml. |
Purification | Immunoaffinity chromatography |
Conjugation | Unconjugated |
Storage Condition | Store lyophilized at 2-8°C for 6 months or at -20°C long term. After reconstitution store the antibody undiluted at 2-8°C for one month or (in aliquots) at -20°C long term. Avoid repeated freezing and thawing. |
Gene Name | apolipoprotein E |
Database Link | |
Background | Apolipoprotein E is essential for the normal catabolism of triglyceride rich lipoprotein constituents. The apolipoprotein E gene is mapped to chromosome 19 in a cluster with APOC1 and APOC2. Defects in Apolipoprotein E result in familial dysbetalipoproteinemia, or type III hyperlipoproteinemia (HLP III), in which increased plasma cholesterol and triglycerides are the consequence of impaired clearance of chylomicron and VLDL remnants. Mutations in the APOE gene confer susceptibility to Alzheimer's disease by affecting amyloid-beta deposition. |
Synonyms | ApoE, Apo-E |
Note | Centrifuge vial prior to opening. |
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