ITT1708
ITT1708
- Catalog: ITT1708
- Gene/Protein: EFEMP1
- Product Description: Immunotag™ Fibulin-3 Polyclonal Antibody
385.0000
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Antibody Specification | |
Datasheet | |
Target Protein | Fibulin-3 |
Clonality | Polyclonal |
Storage/Stability | -20°C/1 year |
Application | WB,IHC-p,ELISA |
Recommended Dilution | Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/10000. Not yet tested in other applications. |
Concentration | 1 mg/ml |
Reactive Species | Human,Mouse,Rat |
Host Species | Rabbit |
Immunogen | Synthesized peptide derived from Fibulin-3, at AA range: 80-160 |
Specificity | Fibulin-3 Polyclonal Antibody detects endogenous levels of Fibulin-3 protein. |
Purification | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen |
Form | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
Gene Name | EFEMP1 |
Accession No. | Q12805 Q8BPB5 O35568 |
Alternate Names | EFEMP1; FBLN3; FBNL; EGF-containing fibulin-like extracellular matrix protein 1; Extracellular protein S1-5; Fibrillin-like protein; Fibulin-3; FIBL-3 |
Description | EGF containing fibulin like extracellular matrix protein 1(EFEMP1) Homo sapiens This gene encodes a member of the fibulin family of extracellular matrix glycoproteins. Like all members of this family, the encoded protein contains tandemly repeated epidermal growth factor-like repeats followed by a C-terminus fibulin-type domain. This gene is upregulated in malignant gliomas and may play a role in the aggressive nature of these tumors. Mutations in this gene are associated with Doyne honeycomb retinal dystrophy. Alternatively spliced transcript variants that encode the same protein have been described.[provided by RefSeq, Nov 2009], |
Protein Expression | Brain,Lung,Skin, |
Subcellular Localization | extracellular region,proteinaceous extracellular matrix,extracellular space,extracellular matrix,extracellular exosome, |
Protein Function | Experimental confirmation may be lacking for some isoforms,disease:Defects in EFEMP1 are a cause of Doyne honeycomb retinal dystrophy (DHRD) [MIM:126600]; also known as malattia leventinese (MLVT OR ML). DHRD is an autosomal dominant disease characterized by yellow-white deposits known as drusen that accumulate beneath the retinal pigment epithelium.,online information:Retina International's Scientific Newsletter,similarity:Belongs to the fibulin family.,similarity:Contains 6 EGF-like domains., |
Usage | For Research Use Only! Not for diagnostic or therapeutic procedures. |