Semaphorin 3E (SEMA3E) Antibody

Este producto es parte de SEMA3 - semaphorin 3
Semaphorin 3E (SEMA3E) Antibody
442€ (200 µl)

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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.

Documentos del producto

Instrucciones
Data sheet
Descargar

Especificaciones del producto

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.

Background

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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