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Invitrogen™ TMEM67 Recombinant Rabbit Monoclonal Antibody (23GB4990), Invitrogen™
Rabbit Recombinant Monoclonal Antibody
Brand: Invitrogen™ MA552897
This item is not returnable.
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Description
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).
Specifications
| TMEM67 | |
| Recombinant Monoclonal | |
| Unconjugated | |
| TMEM67 | |
| 5330408M12Rik; B230117O07; b2b1163.1Clo; b2b1291.1Clo; JBTS6; meckel syndrome type 3 protein; Meckel syndrome type 3 protein homolog; Meckelin; Mks3; NPHP11; TMEM67; TNEM67; transmembrane protein 67 | |
| Rabbit | |
| Affinity chromatography | |
| RUO | |
| 313067, 329795, 91147 | |
| -20°C | |
| Liquid |
| Flow Cytometry, Western Blot, Immunocytochemistry | |
| 23GB4990 | |
| PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
| P0C152, Q5HYA8, Q8BR76 | |
| TMEM67 | |
| A synthesized peptide derived from human Meckelin (801-880AA). | |
| 20 μL | |
| Primary | |
| Human, Mouse, Rat | |
| Antibody | |
| IgG |
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