| Catalog No. | Size | Price (USD) |
| 206626-T02-50 | 50 µL | $147.96 |
| 206626-T02-100 | 100 µL | $251.64 |
| 206626-T02-200 | 200 µL | $355.32 |
General Information
| Product name | Anti-ADAMTSL4 Antibody, Rabbit Polyclonal |
| Validated applications | ICC/IF (FAQ Protocol) |
| Species reactivity | Reacts with: Human |
| Specificity | Human ADAMTSL4 |
| Immunogen | E. coli-derived Human ADAMTSL4 fragment |
| Preparation | Produced in rabbits immunized with E. coli-derived Human ADAMTSL4 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-ADAMTSL-4 Antibody; Anti-DKFZP434K1772 Antibody; Anti-ECTOL2 Antibody; Anti-PP1396 Antibody; Anti-TSRC1 Antibody; Anti-UNQ2803/PRO34012 Antibody
Image / Experimental Information
| Image 1 Description | Immunofluorescence staining of ADAMTSL4 in HeLa cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS,blocked with 10% serum, and incubated with rabbit anti-Human ADAMTSL4 polyclonal antibody (dilution ratio 1:200) at 4℃ overnight. Then cells were stained with the Alexa Fluor®488-conjugated Goat Anti-rabbit IgG secondary antibody (green). Positive staining was localized to Nucleus. |
| Image 1 Alt Text | Human ADAMTSL4 Immunofluorescence(IF) 26545 |
| Image 1 URL | Source image |
Background Information
| Description | The ADAMTS (a disintegrin-like and metalloproteinase domain with thrombospondin-type 1 motifs) protein superfamily includes 19 secreted metalloproteases and 7 secreted ADAMTS-like (ADAMTSL) glycoproteins. ADAMTSL4, a secreted glycoprotein, was earlier found to play a critical role in a prognostic signature for primary glioblastoma multiforme (pGBM). ADAMTSL4 mutations seem to be the most common cause of isolated ectoplia lentis (EL) and thus are important concerning the differential diagnosis of connective tissue syndromes with EL as a main feature. |
| References |
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