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          • Primary Antibodies ›
          • CFTR Antibodies

          Invitrogen

          CFTR Polyclonal Antibody

          View all (63) CFTR antibodies

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          Cite CFTR Polyclonal Antibody

          Additional Information:
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          • Antibody Testing Data (3)
          CFTR Antibody in Immunohistochemistry (Paraffin) (IHC (P))
          Group 53 Created with Sketch.
          CFTR Antibody in Immunohistochemistry (Paraffin) (IHC (P))
          Group 53 Created with Sketch.

          FIGURE: 1 / 3

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          CFTR Antibody (PA5149873) in IHC (P)

          Immunohistochemistry analysis of CFTR in paraffin-embedded Human Kidney tissue. Samples were incubated with CFTR Polyclonal (Product # PA5149873) antibody using a dilution of 10 µg/mL, followed by HRP-Linked Caprine Anti-Rabbit IgG (2 µg/mL) and DAB. {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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          CFTR Antibody in Immunohistochemistry (Paraffin) (IHC (P))
          CFTR Antibody in Immunohistochemistry (Paraffin) (IHC (P))
          CFTR Antibody in Western Blot (WB)
          CFTR Polyclonal Antibody

          Product Details

          PA5149873

          Applications
          Tested Dilution
          Publications

          Western Blot (WB)

          0.01-2 µg/mL
          -

          Immunohistochemistry (Paraffin) (IHC (P))

          5-20 µg/mL
          -

          Immunocytochemistry (ICC/IF)

          5-20 µg/mL
          -
          Product Specifications

          Species Reactivity

          Human, Pig

          Host/Isotype

          Rabbit

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          Recombinant Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) (Gln359-Ser858)
          3D Epitope / Immunogen

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Liquid

          Concentration

          0.5 mg/mL

          Amount

          100 µg

          Purification

          Protein A/G

          Storage buffer

          PBS, pH 7.4, with 50% glycerol

          Contains

          0.05% ProClin 300

          Storage conditions

          Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

          Shipping conditions

          Ambient (domestic); Wet ice (international)

          RRID

          AB_3715908

          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.

          References (0)

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          Cite this product

          Bioinformatics

          Protein Aliases: ATP Binding Cassette Superfamily C Member 7 (ABCC7); ATP-binding cassette sub-family C member 7; ATP-binding cassette transporter sub-family C member 7; cAMP-dependent chloride channel; CFTR; Channel conductance-controlling ATPase; cystic fibrosis transmembrane conductance regulating; Cystic fibrosis transmembrane conductance regulator; cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7); cystic fibrosis transmembrane conductance regulator isoform; membrane channel; 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, (Pig) Q6PQZ2

          View more View less

          Entrez Gene ID: (Human) 1080, (Pig) 403154

          View more View less

          Function(s)
          nucleotide binding chloride channel activity channel-conductance-controlling ATPase activity protein binding ATP binding bicarbonate transmembrane transporter activity chloride transmembrane transporter activity isomerase activity ATPase activity chloride channel regulator activity chloride channel inhibitor activity enzyme binding PDZ domain binding anion transmembrane-transporting ATPase activity chaperone binding 14-3-3 protein binding Sec61 translocon complex binding ABC-type transporter activity ATP-binding cassette (ABC) transporter
          Process(es)
          cholesterol biosynthetic process ion transport chloride transport water transport vesicle docking involved in exocytosis bicarbonate transport cholesterol transport ion transmembrane transport response to endoplasmic reticulum stress transepithelial water transport positive regulation of insulin secretion involved in cellular response to glucose stimulus positive regulation of exocytosis sperm capacitation multicellular organismal water homeostasis intracellular pH elevation establishment of localization in cell transmembrane transport membrane hyperpolarization regulation of biological quality positive regulation of enamel mineralization cellular response to cAMP amelogenesis inorganic ion transmembrane transport chloride transmembrane transport positive regulation of voltage-gated chloride channel activity cellular response to forskolin
          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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