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Invitrogen
TMEM67 Polyclonal Antibody
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FIGURE: 1 / 5
TMEM67 Antibody (PA5-141155) in IHC (P)
Product Details
PA5-141155
Species Reactivity
Host/Isotype
Class
Type
Immunogen
Conjugate
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Purification
Storage buffer
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RRID
Target Information
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).
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
References (0)
Bioinformatics
Protein Aliases: Meckel syndrome type 3 protein; Meckel syndrome type 3 protein homolog; Meckelin; Transmembrane protein 67
Gene Aliases: 5330408M12Rik; B230117O07; b2b1163.1Clo; b2b1291.1Clo; JBTS6; MECKELIN; MKS3; NPHP11; TMEM67; TNEM67
UniProt ID: (Human) Q5HYA8, (Mouse) Q8BR76
Entrez Gene ID: (Human) 91147, (Mouse) 329795
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If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
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