ARG46167
anti-FREM2 antibody
anti-FREM2 antibody for Western blot,ICC/IF and Human,Mouse
Overview
| Product Description | Rabbit Polyclonal antibody recognizes FREM2 |
|---|---|
| Tested Reactivity | Hu, Ms |
| Tested Application | ICC/IF, WB |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | IgG |
| Target Name | FREM2 |
| Antigen Species | Human |
| Immunogen | A 19 amino acid synthetic peptide within aa. 1920 - 1970 of human FREM2. |
| Conjugation | Un-conjugated |
| Alternate Names | FREM2; FRAS1 related extracellular matrix protein 2; DKFZp686J0811; DKFZp781I048; KIAA1074; ECM3 homolog; FRAS1-related extracellular matrix protein 2; OTTHUMP00000018288; OTTHUMP00000018289 |
Application Instructions
| Application Suggestion |
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| Application Note | * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
| Purification | Affinity chromatography purified |
|---|---|
| Buffer | PBS and 0.02% Sodium azide. |
| Preservative | 0.02% Sodium azide |
| Concentration | 1 mg/ml |
| Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
| Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
| Database Links |
Swiss-port # Q5SZK8 Human FRAS1-related extracellular matrix protein 2 Swiss-port # Q6NVD0 Mouse FRAS1-related extracellular matrix protein 2 |
|---|---|
| Gene Symbol | FREM2 |
| Gene Full Name | FRAS1 related extracellular matrix protein 2 |
| Background | This gene encodes a membrane protein that belongs to the FRAS1 family. This extracellular matrix protein is thought to be required for maintaining the integrity of the skin epithelium and the differentiated state of renal epithelia. The protein localizes to the basement membrane, forming a ternary complex that plays a role in epidermal-dermal interactions during morphogenetic processes. Mutations in this gene are associated with Fraser syndrome. [provided by RefSeq, Jul 2008] |
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