Semaphorin 3E (SEMA3E) Antibody
442€ (200 µl)
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935106861
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name
Semaphorin 3E (SEMA3E) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx433260
tested applications
P-ELISA, IHC, IF/ICC, FCM
Description
SEMA3E Antibody is a Goat Polyclonal antibody against SEMA3E.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Target: Semaphorin 3E (SEMA3E) Immunogen: abx269636 - C-Terminus: C-KPEHYRLPRHTLDS |
| Host | Goat |
| Reactivity | Human |
| Assay Type | Concentration: 0.5 mg/ml |
| Recommended Dilution | P-ELISA: 1/64000. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide. |
| Size 1 | 200 µl |
| Form | Liquid |
| Tested Applications | P-ELISA, IHC, IF/ICC, FCM |
| Buffer | Tris saline, pH 7.3, containing 0.02% sodium azide and 0.5% bovine serum albumin. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| Gene ID | 9723 |
| NCBI Accession | NP_036563.1 |
| Alias | SEMAH,coll-5,M-SEMAH,M-SemaK,Semaphorin-3E |
| Background | Antibody anti-SEMA3E |
| Status | RUO |
| Note | THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION. |
Descripción
SEMA3E (Semaphorin 3E) stands out for its dual roles in cellular attraction and repulsion, depending on the receptor context. It binds to plexin D1 as its primary receptor, modulating endothelial cell migration, angiogenesis, and neuronal pathfinding. SEMA3E is unique in its receptor-independent signaling pathways, contributing to its versatile biological functions. In cancer, SEMA3E often exhibits a pro-metastatic role, facilitating tumor cell invasion and vascular remodeling. Its aberrant expression is implicated in aggressive tumor phenotypes, making it a target of interest for anticancer therapies aimed at modulating its signaling pathways.
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