| No | Size | Price | Availability | |
| ARP30008-61 | 50ul | 1500.00 | In Stock |  |
| ARP30008-61 | 100ul | 2000.00 | In Stock | |
| Source: | Rabbit | Gene Id: | 30008 |
| Isotype: | IgG | Swiss Prot: | O95967 |
| purity: | Affinity purification |
| Background: |
| Defects in EFEMP2 are a cause of cutis laxa autosomal recessive type 1 (ARCL1) [MIM:219100]. Hereditary cutis laxa refers to a heterogeneous group of connective tissue disorders characterized by cutaneous abnormalities and variable systemic manifestations. The most constant clinical feature is loose skin, sagging over the face and trunk. |
| Reactivity | Human |
| Tested applications | WB IHC IF ICC |
| Clonality | Polyclonal Antibody |
| Calculated MW | 50 kDa |
| Recommended Dilutions |
WB 1:500-1:1000
IHC 1:50-1:200
IF 1:100-1:500
ICC 1:100-1:500
|
| Immunogen | A synthetic peptide |
| Storage | Store at -20°C or -80°C in PBS with 0.02% sodium azide and 50% glycerol. Avoid freeze/thaw cycles. |
| Synonym | EGF-containing fibulin-like extracellular matrix protein 2, FBLN4 |
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