Products Antibodies Monoclonal Antibodies Anti-Fukutin Monoclonal Antibody for WB, IHC-P, ELISA - O75072

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Monoclonal Antibodies

Anti-Fukutin Monoclonal Antibody for WB, IHC-P, ELISA - O75072

Item Number : CM0003610

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Application
WB, IHC-P, ELISA
Cross Reactivity
Human, Mouse, Rat
Protein Weight
54kDa
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Core Product Specifications and Parameters

Parameter Value
Product Name Fukutin Rabbit mAb
Remarks/Alias FCMD; CMD1X; LGMD2M; MDDGA4; MDDGB4; MDDGC4; LGMDR13; Fukutin
Species Human
GeneID (Human) 2218
GeneID 2218
Immunogen Synthetic Peptide|A synthetic peptide corresponding to a sequence within amino acids 362-461 of human Fukutin (O75072).
Source Rabbit
Category Monoclonal Antibodies
Application WB, IHC-P, ELISA
Cross Reactivity Human, Mouse, Rat
SWISS O75072
Protein Weight 54kDa
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Biological Background: Fukutin Function and Localization

  • FKTN encodes ribitol-5-phosphate transferase FKTN (Fukutin), a transmembrane protein that catalyzes the transfer of a ribitol-phosphate from CDP-ribitol to the phosphorylated O-mannosyl trisaccharide on alpha-dystroglycan (DAG1), initiating the ribitol 5-phosphate tandem repeat essential for ligand binding. Related references: PMID:26923585 PMID:27194101 PMID:29477842 PMID:17034757 PMID:25279699
  • FKTN is required for normal localization of POMGNT1 in Golgi membranes and for normal POMGNT1 activity, and may interact with a large complex reinforcing muscle membrane integrity. Related references: PMID:17034757 PMID:25279699
  • Localizes to the Golgi apparatus membrane, with additional presence in the cytoplasm and nucleus, consistent with its role in glycosylation and potential nuclear functions.
  • Widely expressed with highest levels in brain, heart, pancreas, and skeletal muscle; expressed in neurons and retina, but not in glial cells, suggesting a role in neuronal development and function. Related references: PMID:29416295 PMID:11115853
  • Mutations in FKTN cause a spectrum of dystroglycanopathies including Fukuyama-type congenital muscular dystrophy (FCMD), limb-girdle muscular dystrophy, cardiomyopathy, and lissencephaly, highlighting its critical role in muscle and brain development.
  • Belongs to the fukutin family and is characterized by a signal-anchor and a transmembrane helix, important for its membrane insertion.
  • The protein weight is approximately 54 kDa (UniProt: 53724 Da), consistent with the observed band in Western blot applications.

Experimental Guidance and Technical Tips

  • For Western blot (WB), consider loading protein from human, mouse, or rat tissue lysates (brain, skeletal muscle, heart) and use a molecular weight marker to confirm the band at ~54 kDa.
  • When performing immunohistochemistry on paraffin-embedded sections (IHC-P), antigen retrieval and appropriate positive controls (e.g., human brain or muscle tissue) are recommended; negative controls should include glial-rich regions.
  • In ELISA, the antibody may be used for detection of recombinant or native FKTN; pre-coat the antigen under optimized conditions and validate with known positive/negative samples.
  • Given the cross-reactivity with mouse and rat, verify reactivity in the intended model system by including appropriate positive and negative controls.

CamelBio: Your One-Stop Sourcing Bridge

CamelBio provides diagnostic manufacturers and research laboratories with one-stop access to validated IVD raw materials, including monoclonal antibodies like this anti-Fukutin antibody for dystroglycanopathy and neurological disorder research. Beyond individual reagents, we supply optimized antibody pairs, bulk ancillary reagents, and can source rare-target raw materials to streamline your assay development. Our expertise supports every stage from concept to clinic, ensuring reliable procurement for your diagnostic pipeline.

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Product Datasheet

Anti-Fukutin Monoclonal Antibody for WB, IHC-P, ELISA - O75072


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