購(gòu)物車
幫助
021-54845833/15800441009
|
Background: |
The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6). |
|
Applications: |
ELISA, WB, IHC |
|
Name of antibody: |
TMEM67 |
|
Immunogen: |
Fusion protein of human TMEM67 |
|
Full name: |
transmembrane protein 67 |
|
Synonyms: |
MKS3; JBTS6; NPHP11; TNEM67; MECKELIN |
|
SwissProt: |
Q5HYA8 |
|
ELISA Recommended dilution: |
5000-10000 |
|
IHC positive control: |
Human liver cancer and Human brain |
|
IHC Recommend dilution: |
20-100 |
|
WB Predicted band size: |
112 kDa |
|
WB Positive control: |
Human kidney tissue and A549 cell lysates |
|
WB Recommended dilution: |
200-1000 |
