Catalog_no | AN3258 |
Product_name | ATL2 rabbit pAb |
Category | 抗原抗体 |
Applications | WB |
Reactivity | Human, Mouse |
Size | 100μg/50μg/20μg |
Price | 2000.00/1100.00/500.00 |
Gene_name | ADAMTSL2 KIAA0605 |
Protein_name | ATL2 |
Human swiss prot no | 9719 |
Human swiss prot no | Q86TH1 |
Mouse gene id | 77794 |
Mouse swiss prot no | Q7TSK7 |
immunogen | Synthesized peptide derived from human ATL2 |
Specificity | This antibody detects endogenous levels of ATL2 at Human/Mouse |
Formulation | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.216% sodium azide. |
Source | Rabbit |
Dilution | WB 1:500-2000 |
Purification | The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen. |
Concentration | 1 mg/ml |
Storage_stability | -20°C/1 year |
othername | ADAMTS-like protein 2 (ADAMTSL-2) |
Observed_band | 105KD |
Background | This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) and ADAMTS-like protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The protein encoded by this gene lacks the protease domain, and is therefore of a member of the the ADAMTS-like protein subfamily. It is a secreted glycoprotein that binds the cell surface and extracellular matrix; it also interacts with latent transforming growth factor beta binding protein 1. Mutations in this gene have been associated with geleophysic dysplasia. [provided by RefSeq, Feb 2009], |
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