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Invitrogen™ TMEM67 Polyclonal Antibody

Rabbit Polyclonal Antibody
Brand: Invitrogen™ PA599981
This item is not returnable.
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Description
Antibody detects endogenous levels of total MKS3.
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 | |
| Polyclonal | |
| 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 | |
| 329795, 91147 | |
| -20°C | |
| Liquid |
| Immunohistochemistry (Paraffin), Western Blot | |
| 1 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
| Q5HYA8, Q8BR76 | |
| TMEM67 | |
| A synthesized peptide derived from human TMEM67(Accession Q5HYA8), corresponding to amino acid residues H626-E676. | |
| 100 μL | |
| Primary | |
| Human, Mouse | |
| Antibody | |
| IgG |
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