CFTR recombinant monoclonal antibody, clone CFTR/1775R
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Specifications
Product Description
Rabbit recombinant monoclonal antibody raised against synthetic peptide corresponding to amino acids 258-385 of the human CFTR protein.
Antibody Species
Rabbit
Immunogen
Original antibody is raised against a synthetic peptide corresponding to amino acids 258-385 of the human CFTR protein
Reactivity
Human
Form
Liquid
Conjugation
Unconjugated
Purification
Protein A affinity chromatography
Concentration
0.2 mg/mL
Isotype
IgG
Recommend Usage
Immunofluorescence (0.5-1 ug/mL)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)(1-2 ug/mL for 30 min at RT)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, 0.1 mg/ml BSA, 0.05% sodium azide
Storage Instruction
Store at 2~8°C.
Aliquot to avoid repeated freezing and thawing.Note
Optimal dilutions for each application to be determined by the researcher
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Applications
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemistry (Formalin-fixed paraffin-embedded sections) of human pancreas with anti-CFTR recombinant monoclonal antibody, clone CFTR/1775R (Cat # RAB03808).Immunofluorescence
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Gene Info — CFTR
Entrez GeneID
1080Protein Accession#
P13569Gene Name
CFTR
Gene Alias
ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR, dJ760C5.1
Gene Description
cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
Gene Ontology
HyperlinkGene Summary
This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily that is involved in multi-drug resistance. The encoded protein functions as a chloride channel and controls the regulation of other transport pathways. Mutations in this gene are associated with the autosomal recessive disorders cystic fibrosis and congenital bilateral aplasia of the vas deferens. Alternatively spliced transcript variants have been described, many of which result from mutations in this gene. [provided by RefSeq
Other Designations
ATP-binding cassette sub-family C, member 7|cystic fibrosis transmembrane conductance regulator
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Interactomes
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Pathways
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Diseases
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