TMEM67 产品
(Transmembrane Protein 67 (TMEM67))
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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). [provided by RefSeq, Nov 2008].
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TMEM67 抗体
High quality antibodies with extensive validation data.
Recommended TMEM67 抗体
Product
Reactivity
Application
Validations
Cat. No.
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Datasheet
Reactivity
Human
Application
ELISA, IHC, IF
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Cat. No.
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Quantity
100 μg
Datasheet
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Reactivity
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Application
WB, IHC
Validations
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Cat. No.
ABIN6263272
Quantity
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Datasheet
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Reactivity
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Application
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Validations
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Cat. No.
ABIN347657
Quantity
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Datasheet
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Latest Publications for our TMEM67 Products
: "Meckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndrome." in: PLoS ONE, Vol. 8, Issue 3, pp. e59306, (2013) (PubMed).Synonyms and alternative names related to TMEM67
transmembrane protein 67 (TMEM67), transmembrane protein 67 (tmem67), transmembrane protein 67 (Tmem67), 5330408M12Rik, b2b1163.1Clo, b2b1291.1Clo, B230117O07, JBTS6, MECKELIN, MKS3, NPHP11, TNEM67, WpkProtein level used designations for TMEM67
- transmembrane protein 67
- mks3
- meckelin-like
- Meckelin-like
- Meckelin
- meckel syndrome type 3 protein
- meckel syndrome type 3 protein homolog
- Meckel syndrome type 3 protein homolog
- Wistar polycystic kidney
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