CFTR anticorps (AA 1339-1351)
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- Antigène Voir toutes CFTR Anticorps
- CFTR (Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR))
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Épitope
- AA 1339-1351
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Reactivité
- Humain, Mouton
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp CFTR est non-conjugé
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Application
- Immunohistochemistry (IHC)
- Immunogène
- Polyclonal antibody produced in rabbits immunizing with a synthetic peptide corresponding to residues 1339-1351 of human CFTR (Cystic fibrosis transmembrane conductance regulator)
- Top Product
- Discover our top product CFTR Anticorps primaire
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- Restrictions
- For Research Use only
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- Stock
- -20 °C
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- Antigène
- CFTR (Cystic Fibrosis Transmembrane Conductance Regulator (ATP-Binding Cassette Sub-Family C, Member 7) (CFTR))
- Autre désignation
- CFTR (CFTR Produits)
- Synonymes
- anticorps ABC35, anticorps ABCC7, anticorps CF, anticorps CFTR/MRP, anticorps MRP7, anticorps TNR-CFTR, anticorps dJ760C5.1, anticorps CFTR, anticorps AW495489, anticorps Abcc7, anticorps RGD1561193, anticorps abc35, anticorps abcc7, anticorps cftr/mrp, anticorps mrp7, anticorps tnr-cftr, anticorps xcftr, anticorps si:dkey-270i2.2, anticorps cystic fibrosis transmembrane conductance regulator, anticorps cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7), anticorps CFTR, anticorps cftr-A, anticorps Cftr, anticorps cftr
- Sujet
- CFTR (Cystic fibrosis transmembrane conductance regulator) is involved in the transport of chloride ions and binds SLC9A3R1. CFTR is an integral membrane protein. Defects in CFTR are the cause of cystic fibrosis (CF) , also known as mucoviscidosis. It belongs to the ABC transporter family and MRP subfamily.
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