FKTN polyclonal antibody
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of human FKTN.
Immunogen
A synthetic peptide corresponding to N-terminus of human FKTN.
Sequence
TAFALQYHLWKNEEGWFRIAENMGFQCLKIESKDPRLDGIDSLSGTEIPL
Host
Rabbit
Theoretical MW (kDa)
51
Reactivity
Human
Form
Liquid
Purification
Protein A purification
Recommend Usage
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (4-8 ug/mL)
Western Blot (5 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (2% sucrose, 0.09% sodium azide).
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Cell lysate)
Western Blot analysis of Jurkat cell lysate with FKTN polyclonal antibody (Cat # PAB30079) at 5 ug/mL working concentration.Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human muscle with FKTN polyclonal antibody (Cat # PAB30079) at 4-8 ug/mL working concentration. -
Gene Info — FKTN
Entrez GeneID
2218GeneBank Accession#
NM_001079802Protein Accession#
NP_001073270;O75072Gene Name
FKTN
Gene Alias
CMD1X, FCMD, LGMD2M, MGC126857, MGC134944, MGC134945, MGC138243
Gene Description
fukutin
Gene Ontology
HyperlinkGene Summary
The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq
Other Designations
Fukuyama type congenital muscular dystrophy protein|OTTHUMP00000021841
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Interactome
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Disease
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