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          Clicking the images or links will redirect you to a website hosted by BenchSci that provides third-party scientific content. Neither the content nor the BenchSci technology and processes for selection have been evaluated by us; we are providing them as-is and without warranty of any kind, including for use or application of the Thermo Fisher Scientific products presented.

          • Primary Antibodies ›
          • CFTR Antibodies

          Proteintech

          CFTR Polyclonal Antibody

          5 References
          View all (58) CFTR antibodies

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          Cite CFTR Polyclonal Antibody

          Additional Information:
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          • Antibody Testing Data (6)
          CFTR Antibody in Immunocytochemistry (ICC/IF)
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          CFTR Antibody in Immunocytochemistry (ICC/IF)
          Group 53 Created with Sketch.

          FIGURE: 1 / 6

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          CFTR Antibody (20738-1-AP) in ICC/IF

          Immunofluorescent analysis of HepG2 cells using 20738-1-AP (CFTR antibody) at dilution of 1:50 and Alexa Fluor 488-conjugated AffiniPure Goat Anti-Rabbit IGG (H+L). {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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          CFTR Antibody in Immunocytochemistry (ICC/IF)
          CFTR Antibody in Immunohistochemistry (Paraffin) (IHC (P))
          CFTR Antibody in Immunohistochemistry (Paraffin) (IHC (P))
          CFTR Antibody in Immunohistochemistry (Paraffin) (IHC (P))
          CFTR Antibody in Immunohistochemistry (Paraffin) (IHC (P))
          CFTR Antibody in Flow Cytometry (Flow)

          Product Details

          20738-1-AP

          Applications
          Tested Dilution
          Publications

          Western Blot (WB)

          Assay-dependent
          View 3 publications 3 publications

          Immunohistochemistry (Paraffin) (IHC (P))

          1:20-1:200
          -

          Immunocytochemistry (ICC/IF)

          1:50-1:500
          View 2 publications 2 publications

          Flow Cytometry (Flow)

          Assay-dependent
          -
          Product Specifications

          Species Reactivity

          Human

          Published species

          Mouse

          Host/Isotype

          Rabbit / IgG

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          Peptide

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Liquid

          Concentration

          0.37 mg/mL

          Purification

          Antigen affinity chromatography

          Storage buffer

          PBS, pH 7.3, with 50% glycerol

          Contains

          0.02% sodium azide

          Storage conditions

          -20°C

          Shipping conditions

          Wet ice (domestic); Dry ice (international)

          Target Information

          Cystic Fibrosis (CF) is a common lethal genetic disease caused by mutations of the gene coding for the cystic fibrosis transmembrane conductance factor, a cAMP regulated chloride channel. Approximately 70% of all CF cases share the deletion of a phenylalanine at position 508 (delta F508) which results in abnormal chloride transport. Since the CF mutation is lethal, most often by lung and liver disease, it raises the question of why this genetic disease remains as common as it is. One possible explanation is that Salmonella typhi has been shown to use CFTR to enter intestinal epithelial cells and that delta F508 heterozygote and homozygote mice showed 86% and 100% reductions in S. typhi intestinal submucosal uptake.

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

          Bioinformatics

          Protein Aliases: ATP Binding Cassette Superfamily C Member 7 (ABCC7); ATP-binding cassette sub-family C member 7; cAMP-dependent chloride channel; CFTR; Channel conductance-controlling ATPase; Cystic fibrosis transmembrane conductance regulator; cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7); tcag7.78; TNR CFTR

          View more View less

          Gene Aliases: ABC35; ABCC7; CF; CFTR; CFTR/MRP; dJ760C5.1; MRP7; TNR-CFTR

          View more View less

          UniProt ID: (Human) P13569

          View more View less

          Entrez Gene ID: (Human) 1080

          View more View less

          Function(s)
          ATP-binding and phosphorylation-dependent chloride channel activity chloride channel activity channel-conductance-controlling ATPase activity protein binding ATP binding bicarbonate transmembrane transporter activity chloride transmembrane transporter activity chloride channel regulator activity chloride channel inhibitor activity enzyme binding PDZ domain binding anion transmembrane-transporting ATPase activity ATP-binding cassette (ABC) transporter
          Process(es)
          cholesterol biosynthetic process transport vesicle docking involved in exocytosis respiratory gaseous exchange bicarbonate transport cholesterol transport positive regulation of insulin secretion involved in cellular response to glucose stimulus positive regulation of exocytosis sperm capacitation intracellular pH elevation transmembrane transport membrane hyperpolarization cellular response to cAMP positive regulation of cyclic nucleotide-gated ion channel activity chloride transmembrane transport positive regulation of voltage-gated chloride channel activity
          It has to be done as per old AB suggested Products section.
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          If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

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