TMEM67 antibody (Center)
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- Target See all TMEM67 Antibodies
- TMEM67 (Transmembrane Protein 67 (TMEM67))
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Binding Specificity
- Center
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This TMEM67 antibody is un-conjugated
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Application
- Western Blotting (WB)
- Cross-Reactivity
- Human
- Characteristics
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Rabbit polyclonal antibody to Meckelin (transmembrane protein 67)
meckelin isoform 1 antibody [N2C1], Internal - Purification
- Purified by antigen-affinity chromatography.
- Immunogen
- Recombinant protein encompassing a sequence within the center region of human meckelin isoform 1. The exact sequence is proprietary.
- Isotype
- IgG
- Top Product
- Discover our top product TMEM67 Primary Antibody
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- Application Notes
- WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- Comment
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Positive Control: H1299
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal
- Preservative
- Thimerosal (Merthiolate)
- Precaution of Use
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- 4 °C,-20 °C
- Storage Comment
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- Target
- TMEM67 (Transmembrane Protein 67 (TMEM67))
- Alternative Name
- transmembrane protein 67 (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
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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).
Cellular Localization: Cell membrane, Multi-pass membrane protein - Molecular Weight
- 112 kDa
- Gene ID
- 91147
- UniProt
- Q5HYA8
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