Leucine-Rich Repeat-Containing Protein 4B (LRRC4B) Antibody

Este producto es parte de LRRC - Leucine-rich repeat-containing protein
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292.5€ (80 µl)

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935106861
info@markelab.com
name
Leucine-Rich Repeat-Containing Protein 4B (LRRC4B) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx025564
tested applications
ELISA, WB

Description

LRRC4B Antibody is a Rabbit Polyclonal antibody against LRRC4B.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Leucine-Rich Repeat-Containing Protein 4B (LRRC4B)
Host
Rabbit
Reactivity
Human, Mouse
Recommended Dilution
WB: 1/1000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified through a protein A column, followed by peptide affinity purification.
Size 1
80 µl
Size 2
400 µl
Form
Liquid
Tested Applications
ELISA, WB
Buffer
PBS containing 0.09% sodium azide.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q9NT99
Gene ID
94030
Alias
LRRC4B, LRIG4,Netrin-G3 ligand ,NGL-3
Background
Antibody anti-LRRC4B
Status
RUO

Descripción

LRRC4B, also known as netrin-G ligand 3 (NGL-3), is a transmembrane protein containing leucine-rich repeats that mediate synaptic adhesion, neuronal development, and signaling processes. It interacts with netrin-G proteins to form trans-synaptic connections that promote synapse formation, stabilization, and excitatory synaptic transmission in the central nervous system. LRRC4B is highly expressed in the brain, particularly in regions regulating learning, memory, and synaptic plasticity, where it supports the organization of neural circuits and dendritic spine maturation. Dysregulation of LRRC4B is associated with neurodevelopmental disorders, including autism spectrum disorders (ASD) and intellectual disabilities, due to impaired synaptic connectivity and function. Functional studies in knockout models demonstrate synaptic defects, abnormal neuronal morphology, and reduced synaptic transmission, emphasizing its essential role in maintaining excitatory synapse structure and function during brain development.

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