B- And T-Lymphocyte Attenuator (BTLA) Antibody

Este producto es parte de BTLA - B and T lymphocyte associated
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260€ (50 µl)

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935106861
info@markelab.com
name
B- And T-Lymphocyte Attenuator (BTLA) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx339208
tested applications
ELISA, IHC

Description

BTLA Antibody is a Rabbit Polyclonal against BTLA.

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryPrimary Antibodies
Immunogen TargetB- And T-Lymphocyte Attenuator (BTLA)
HostRabbit
ReactivityHuman
Recommended DilutionELISA: 1/1000 - 1/2000, IHC: 1/25 - 1/100. Optimal dilutions/concentrations should be determined by the end user.
ClonalityPolyclonal
ConjugationUnconjugated
IsotypeIgG
PurificationAntigen Affinity Chromatography.
Size 150 µl
Size 2100 µl
FormLiquid
Tested ApplicationsELISA, IHC
BufferPBS, pH 7.4, containing 0.05% NaN3 and 40% Glycerol.
AvailabilityShipped within 5-10 working days.
StorageAliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry IceNo
UniProt IDQ7Z6A9
Gene ID151888
AliasB- and T-lymphocyte attenuator,BTLA1,CD272,
BackgroundAntibody anti-BTLA
StatusRUO

Descripción

B and T Lymphocyte Attenuator (BTLA) is an immunoglobulin superfamily receptor expressed on various immune cells, notably B cells, T cells, macrophages, and dendritic cells. BTLA is a crucial immune checkpoint molecule that modulates immune responses by interacting with its ligand, Herpesvirus entry mediator (HVEM), to maintain immune homeostasis and prevent overactivation that could lead to autoimmune responses. As an immune checkpoint, BTLA is part of a larger family of inhibitory receptors, such as PD-1 and CTLA-4, that regulate immune cell activity to mitigate excessive inflammatory responses. However, BTLA has distinct binding affinities and structural features, which influence its role in modulating immune responses, inflammation, and tolerance. BTLA's interaction with HVEM is unique among immune checkpoint pathways because HVEM also binds several other ligands, including LIGHT (TNFSF14) and lymphotoxin α. This interaction allows for complex regulatory functions, enabling BTLA to provide inhibitory signals that dampen T cell receptor (TCR) and B cell receptor (BCR) signaling. Such regulation is vital in preventing autoimmunity and controlling immune responses in infection, inflammation, and cancer, where immune modulation can prevent tumor growth but also, if dysregulated, may suppress necessary immune responses against cancer cells.

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