Application
C1orf187 Antibody (C-term) western blot analysis in mouse spleen,stomach tissue lysates (35ug/lane).This demonstrates the C1orf187 antibody detected the C1orf187 protein (arrow).| Product Name | C1orf187 Antibody (C-term) |
|---|---|
| Antibody Type | Primary Antibodies |
| Antigen Alias | C1orf187; Draxin; Dorsal repulsive axon guidance protein; Neucrin |
| Clonality | Polyclonal |
|---|---|
| Isotype | Ig |
| Host Species | Rabbit |
| Tested Applications | WB |
| WB:1:100~500 |
|
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Gene Synonyms | C1orf187 |
|---|---|
| Alternative Names | C1orf187 Draxin Dorsal repulsive axon guidance protein Neucrin |
| Molecular Weight(MW) | 38650 Da |
| Function | Chemorepulsive axon guidance protein required for the development of spinal cord and forebrain commissures. Acts as a chemorepulsive guidance protein for commissural axons during development. Able to inhibit or repel neurite outgrowth from dorsal spinal cord. Inhibits the stabilization of cytosolic beta- catenin (CTNNB1) via its interaction with LRP6, thereby acting as an antagonist of Wnt signaling pathway (By similarity) |
| Tissue Specificity | This C1orf187 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 303-333 amino acids from the C-terminal region of human C1orf187. |
| Cellular Localization | Secreted (Probable). |
| Entrez Gene | 374946 |
|---|---|
| Nucleotide Accession | NP_940947.3 |
Application
C1orf187 Antibody (C-term) western blot analysis in mouse spleen,stomach tissue lysates (35ug/lane).This demonstrates the C1orf187 antibody detected the C1orf187 protein (arrow).| Application Notes | WB:1:100~500 |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles. |
| Storage Buffer | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
