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TMEM67 antibody (Isoform 1)
TMEM67
Reactivity: Human
WB
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-TMEM67 Antibody
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Target
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TMEM67
(Transmembrane Protein 67 (TMEM67))
Binding Specificity
All epitopes for TMEM67 antibodies
Isoform 1
Reactivity
All reactivities for TMEM67 antibodies
Human
Host
All hosts for TMEM67 antibodies
Rabbit
Clonality
All clonalities for TMEM67 antibodies
Polyclonal
Conjugate
All conjugates for TMEM67 antibodies
This TMEM67 antibody is un-conjugated
Application
All applications for TMEM67 antibodies
Western Blotting (WB)
Purification
Purified by antigen-affinity chromatography.
Immunogen
Recombinant protein fragment contain a sequence corresponding to a region within amino acids 231 and 480 of Human TMEM67
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Discover our top product TMEM67 Primary Antibody
Alternatives
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Application Details
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Application Notes
Suggested dilutions: Western blotting: 1.500-1.3000
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
Preservative
Thimerosal (Merthiolate)
Precaution of Use
Biohazard Informations: This product contains thimerosal which is hazardous.
Storage
4 °C/-20 °C
Storage Comment
Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
Target Details for TMEM67
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Target
TMEM67
(Transmembrane Protein 67 (TMEM67))
Alternative Name
meckelin (TMEM67 Products )
Synonyms
JBTS6 antibody, MECKELIN antibody, MKS3 antibody, NPHP11 antibody, TNEM67 antibody, 5330408M12Rik antibody, B230117O07 antibody, b2b1163.1Clo antibody, b2b1291.1Clo antibody, Wpk antibody, transmembrane protein 67 antibody, TMEM67 antibody, tmem67 antibody, Tmem67 antibody
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).[provided by RefSeq]
Molecular Weight
112 kDa
Gene ID
91147
NCBI Accession
NP_714915 , NM_153704
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