| Catalog No. | Size | Price (USD) |
| 205647-T08-50 | 50 µL | $147.96 |
| 205647-T08-100 | 100 µL | $251.64 |
| 205647-T08-200 | 200 µL | $355.32 |
General Information
| Product name | Anti-FAM169A Antibody, Rabbit Polyclonal |
| Validated applications | IHC-P (FAQ Protocol) |
| Species reactivity | Reacts with: Human |
| Specificity | Human FAM169A |
| Immunogen | E. coli-derived Human FAM169A fragment |
| Preparation | Produced in rabbits immunized with E. coli-derived Human FAM169A fragment, and purified by antigen affinity chromatography. |
| Source | Polyclonal Rabbit IgG |
| Purification | Protein A & Antigen Affinity |
| Formulation | PBS, pH7.0 with 0.03% Proclin300 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Shipping | This antibody is shipped as liquid solution at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. |
| Storage | This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Avoid repeated freeze-thaw cycles. |
Synonyms: Anti-KIAA0888 Antibody; Anti-SLAP Antibody; Anti-SLAP75 Antibody
Image / Experimental Information
| Image 1 Description | Immunochemical staining of human FAM169A in human testis with rabbit polyclonal antibody at 1:5000 dilution, formalin-fixed paraffin embedded sections. |
| Image 1 Alt Text | Human FAM169A Immunohistochemistry(IHC) 26042 |
| Image 1 URL | Source image |
Background Information
| Description | FAM169A (Family With Sequence Similarity 169 Member A) is located on human chromosome 5q13.3. FAM169A may also be known as SLAP75, soluble lamin-associated protein of 75 kDa, and protein FAM169A. The FAM169A gene is conserved in chimpanzee, Rhesus monkey, dog, cow, mouse, rat, and frog. 200 organisms have orthologs with human gene FAM169A.The FAM169A protein is broadly expressed in brain, testis and other tissues. Structurally, the protein is reported to be 75 kD in mass. FAM169A is associated with some diseases, such as Emery-Dreifuss Muscular Dystrophy 4, Autosomal Dominant. |
| References |
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