TMED9 antibody

Este producto es parte de TMED - Transmembrane emp24 domain-containing
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935106861
info@markelab.com
name
TMED9 antibody
category
Primary Antibodies
provider
FineTest
reference
FNab08741
tested applications
ELISA, WB, IF, IHC

Description

Appears to be involved in vesicular protein trafficking, mainly in the early secretory pathway. In COPI vesicle-mediated retrograde transport involved in the coatomer recruitment to membranes of the early secretory pathway. Increases coatomer-dependent activity of ARFGAP2. Thought to play a crucial role in the specific retention of p24 complexes in cis-Golgi membranes; specifically contributes to the coupled localization of TMED2 and TMED10 in the cis-Golgi network. May be involved in organization of intracellular membranes, such as of the ER-Golgi intermediate compartment and the Golgi apparatus. Involved in ER localization of PTPN2 isoform PTPB.

Documents del producto

Instrucciones
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Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
transmembrane emp24 protein transport domain containing 9 (TMED9)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
WB: 1:1000-1:3000; IHC: 1:20-1:200; IF: 1:10-1:100
Clonality
polyclonal
Conjugation
Unconjugated
Isotype
IgG
Observed MW
27 kDa
Purity
≥95% as determined by SDS-PAGE
Purification
Immunogen affinity purified
Size 1
100µg
Form
liquid
Tested Applications
ELISA, WB, IF, IHC
Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months(Avoid repeated freeze / thaw cycles.)
UniProt ID
Q9BVK6
Gene ID
54732
Alias
GMP25, HSGP25L2G, p24a2, p24alpha2, p25,GP25L2
Background
Antibody anti-TMED9
Status
RUO
Note
Mol. Weight 27 kDa

Descripción

TMED9 is a critical member of the p24 protein family that regulates protein trafficking between the endoplasmic reticulum (ER), ER-Golgi intermediate compartment (ERGIC), and the Golgi apparatus. It functions as a cargo receptor, facilitating the export of correctly folded proteins through COPII-coated vesicles and supporting retrograde retrieval via COPI transport machinery. TMED9 also regulates protein quality control, ensuring proper sorting, maturation, and recycling of secretory and membrane-bound proteins. It plays additional roles in signaling pathways, including Wnt and growth factor signaling, by modulating receptor trafficking and localization at the plasma membrane. TMED9 is widely expressed, particularly in secretory cells, immune tissues, and proliferative compartments. Dysregulation of TMED9 has been associated with cancers and metabolic diseases, where altered trafficking dynamics impair protein secretion and receptor signaling. Knockdown studies reveal defects in vesicle formation, impaired Golgi organization, and disrupted cellular homeostasis, emphasizing its essential role in coordinating vesicular transport, protein quality control, and signaling regulation.

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Appears to be involved in vesicular protein trafficking, mainly in the early secretory pathway. In COPI vesicle-mediated retrograde transport involved in the coatomer recruitment to membranes of the early secretory pathway. Increases coatomer-dependent activity of ARFGAP2. Thought to play a crucial role in the specific retention of p24 complexes in cis-Golgi membranes; specifically contributes to the coupled localization of TMED2 and TMED10 in the cis-Golgi network. May be involved in organization of intracellular membranes, such as of the ER-Golgi intermediate compartment and the Golgi apparatus. Involved in ER localization of PTPN2 isoform PTPB.

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