Anoctamin 6 antibody (2nd Extracellular Loop)
Quick Overview for Anoctamin 6 antibody (2nd Extracellular Loop) (ABIN7884761)
Target
See all Anoctamin 6 (ANO6) AntibodiesReactivity
Host
Clonality
Conjugate
Application
Grade
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Binding Specificity
- 2nd Extracellular Loop, AA 487-500
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Purpose
- A Rabbit Polyclonal Antibody to Anoctamin-6 Channel
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Predicted Reactivity
- Mouse,rat - 12,14 amino acid residues identical
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Purification
- Affinity purified on immobilized antigen.
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Immunogen
- (C)KLPKNINGTDPIQK, corresponding to amino acid residues 487-500 of human ANO6
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Isotype
- IgG
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Application Notes
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WB: 1:200
FC: 5 μg per reaction
ICC: The optimal concentration should be determined by the user
IHC: The optimal concentration should be determined by the user
IP: The optimal concentration should be determined by the user
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Comment
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Negative Control: (ABIN7234747)
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- 0.2 mL double distilled water (DDW)
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Concentration
- 1 mg/mL
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Buffer
- PBS pH 7.4
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Preservative
- Without preservative
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Storage
- -20 °C
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Storage Comment
- The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20°C
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- Anoctamin 6 (ANO6)
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Alternative Name
- ANO6
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Background
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Synonyms: ANO6, Transmembrane protein 16F, TMEM16F, Small-conductance calcium-activated nonselective cation channel, SCAN channel
Description: Anoctamin-6 (ANO6, TMEM16F) is a member of the Anoctamin chloride channel family. This family includes 10 proteins: ANO1-ANO10 that are encoded by the conserved TMEM16A-K genes. Anoctamin-6 acts as calcium (Ca2+)-activated chloride (Cl-) channel. It generates an outwardly rectifying Cl- current when activated by a large increase in local intracellular Ca2+ concentrations1. ANO6 structure includes eight transmembrane domains and cytosolic amino- and carboxyl termini. There is a high sequence identity in the putative transmembrane domains and more divergent in other regions2,3.ANO6 has also been shown to operate as a Ca2+-activated phospholipid scramblase resulting in movement of phosphatidylserine from the inner to the outer leaflet of the plasma membrane bilayer. ANO6 is also involved in bone mineralization, cell volume regulation, cell proliferation and apoptosis1,2. ANO6 is expressed in cyst-forming epithelial cells together with ANO1.A mutation in the ANO6 gene is linked to Scott Syndrome, a rare inherited bleeding disorder, characterized by altered Ca2+-dependent platelet signaling with defective phosphatidylserine exposure and microparticle formation. Deletion of ANO6 in mice shows reduced skeleton size, skeletal deformities, and mineralization defects4,5.
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Gene ID
- 196527
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UniProt
- Q4KMQ2
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Pathways
- SARS-CoV-2 Protein Interactome
Target
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