Signaling Threshold Regulating Transmembrane Adaptor 1 (SIT1) Antibody

Este producto es parte de SIT1 - Signaling threshold-regulating transmembrane adapter 1
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292.5€ (80 µl)

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935106861
info@markelab.com
name
Signaling Threshold Regulating Transmembrane Adaptor 1 (SIT1) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx029063
tested applications
ELISA, WB

Description

Negatively regulates TCR (T-cell antigen receptor) mediated signaling in T-cells. Involved in positive selection of T-cells.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Signaling Threshold Regulating Transmembrane Adaptor 1 (SIT1)
Host
Rabbit
Reactivity
Human
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
Q9Y3P8
Alias
SIT1, SIT, SIT-R, signaling threshold regulating transmembrane adaptor 1
Background
Antibody anti-SIT1
Status
RUO

Descripción

Signaling Threshold-Regulating Transmembrane Adapter 1 (SIT1), also known as SIT, is an immunoregulatory protein primarily expressed in T cells. It acts as a transmembrane adaptor involved in modulating T-cell receptor (TCR) signaling by interacting with key intracellular signaling molecules such as Src family kinases and SH2 domain-containing phosphatases. SIT1 fine-tunes immune responses by negatively regulating TCR-mediated activation, thus maintaining immune tolerance and preventing overactivation that could lead to autoimmune diseases. Its dysregulation is associated with immune disorders and may affect T-cell maturation and peripheral immune homeostasis.

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