+ |
CCL19 | up-regulates activity
binding
|
ACKR4 |
0.653 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268416 |
|
|
Homo sapiens |
U2-OS Cell |
pmid |
sentence |
23341447 |
In the present study, however, we demonstrate for the first time the concentration-dependent recruitment of β-arrestins to the atypical chemokine receptor CCX-CKR upon stimulation with CCL19, CCL21, or CCL25 using three different methodologies in various transfected cell lines. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CCL25 | up-regulates activity
binding
|
ACKR4 |
0.653 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268418 |
|
|
Homo sapiens |
U2-OS Cell |
pmid |
sentence |
23341447 |
In the present study, however, we demonstrate for the first time the concentration-dependent recruitment of β-arrestins to the atypical chemokine receptor CCX-CKR upon stimulation with CCL19, CCL21, or CCL25 using three different methodologies in various transfected cell lines. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CCL21 | up-regulates activity
binding
|
ACKR4 |
0.655 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268417 |
|
|
Homo sapiens |
U2-OS Cell |
pmid |
sentence |
23341447 |
In the present study, however, we demonstrate for the first time the concentration-dependent recruitment of β-arrestins to the atypical chemokine receptor CCX-CKR upon stimulation with CCL19, CCL21, or CCL25 using three different methodologies in various transfected cell lines. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |