| ALX-804-414-C100 | 100 µg | 259.00 USD | ![]() |
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| Purity Detail: | Purified from serum-free cell culture supernatnant by subsequent thiophilic adsorption and size eclusion chromatography. |
| Formulation: | Lyophilized from 1ml 2x PBS, 0.09% sodium azide, PEG and sucrose. |
| Clone: | 19H11 |
| Isotype: | Mouse IgG1 |
| Immunogen: | Synthetic peptide corresponding to N-terminal domain of human β-amyloid. |
| Reconstitution: | Reconstitute with 1ml distilled water (15 min., RT). |
| Specificity: | Recognizes the free N-terminal domain of human β-amyloid. |
| Application: | ELISA (0.05 μg/ml) Immunocytochemistry (0.1-1µg/ml) Western Blot (1µg/ml for HRPO/ECL detection) |
| Long Term Storage: | -20°C |
| Use/Stability: | Reconstituted antibody is stable for 1 year when stored at -80°C. Thaw aliquots at +37°C. Thawed aliquots may be stored at +4°C for up to 3 months. |
| Handling: | After reconstitution, prepare aliquots and freeze in liquid nitrogen. Avoid freeze/thaw cycles. |
| Crossreactivity Proteins: | Shows only minor crossreactions with APP. |
| Miscellaneous/General: | The beta-amyloid peptide (beta A4), proteolytically released from the amyloid precursor protein (APP), is the principal component of senile plaques in Alzheimer's disease. Cleavage of APP by alpha-secretase or alternatively by beta-secretase leads to generation and extracellular release of soluble APP peptides, S-APP-alpha and S-APP-beta, respectively, and the retention of corresponding membrane-anchored C-terminal fragments, C83 and C99. Subsequent processing of C83 by gamma-secretase yields P3 peptides. This is the major secretory pathway and is nonamyloidogenic. Alternatively, presenilin/nicastrin-mediated gamma-secretase processing of C99 releases the amyloid beta proteins, amyloid-beta 40 (Abeta40) and amyloid-beta 42 (Abeta42), major components of amyloid plaques, and the cytotoxic C-terminal fragments, gamma-CTF(50), gamma-CTF(57) and gamma-CTF(59). |

| 20-Sep-10 | |
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