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You are here:Home » Antibodies » Abs to Multi Drug Resistance (MDR) » Anti -CFTR, ID (Cystic Fibrosis Transmembrane Conductance Regulator, ATP-binding Cassette Sub-family C Member 7, Channel Conductance-controlling ATPase, cAMP-dependent Chloride Channel, ABCC7)

Anti -CFTR, ID (Cystic Fibrosis Transmembrane Conductance Regulator, ATP-binding Cassette
Sub-family C Member 7, Channel Conductance-controlling ATPase, cAMP-dependent Chloride
Channel, ABCC7)

Pricing

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Specifications

Clone Host Grade Applications
Polyclonal Rabbit Affinity Purified E B IH
CFTR (Cystic Fibrosis Transmembrane Conductance Regulator), sometimes also referred as ABCC7 (ATP-binding cassette, Subfamily C, Member 7), is a member of the ATP binding cassette (ABC) transporter family. CFTR functions as a chloride channel and controls the regulation of other transport pathways. Homozygous mutations in the CFTR gene cause cystic fibrosis (CF), formerly known as mucoviscidosis, a common hereditary disorder characterized by severe abnormalities in respiratory, digestive and other organ systems. Approximately 70% of the mutations in CF patients correspond to a specific deletion of 3 base pairs, which results in the loss of a phenylalanine at position 508. The approaches aimed to restore the CFTR gene function in CF patients are the subject of intensive research and include the development of gene therapy protocols. In addition to CF syndrome, CFTR mutations were found in patients suffering from bilateral aplasia of the vas deferens (CBAVD). The high frequency of CFTR defects in the human population can be explained by increased resistance to infectious diseases in heterozygous mutation carriers. Alternative splice variants have been described, many of which result from mutations in the CFTR gene.
Catalog #C9040-06B
ApplicationsSuitable for use in ELISA, Western Blot and Immunohistochemistry. Other applications not tested.
Recommended DilutionELISA: 1:1000
Western Blot: 1:500-1:1000
Immunohistochemistry (Formalin fixed paraffin embedded): 10ug/ml
Optimal dilutions to be determined by the researcher.
Storage and StabilityMay be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for at least 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Clone TypePolyclonal
IsotypeIgG
HostRabbit
SourceHuman
Concentration~1mg/ml
FormSupplied as a liquid in PBS (without Mg2+, Ca2+), pH 7.4, 150mM sodium chloride, 0.02% sodium azide, 50% glycerol.
PurityPurified by immunoaffinity chromatography.
ImmunogenSynthetic peptide corresponding to human CFTR.
SpecificityRecognizes human CFTR. Species sequence homology: mouse and rat.
Important NoteThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.


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