Fukutin anticorps (AA 177-206)
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- Antigène Voir toutes Fukutin (FKTN) Anticorps
- Fukutin (FKTN)
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Épitope
- AA 177-206
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp Fukutin est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Purification
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogène
- This FKTN antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 177-206 amino acids from the Central region of human FKTN.
- Isotype
- Ig Fraction
- Top Product
- Discover our top product FKTN Anticorps primaire
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- Indications d'application
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For WB starting dilution is: 1:1000
For IHC-P starting dilution is: 1:10~50 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.5 mg/mL
- Buffer
- Supplied in PBS with 0.09 % (W/V) sodium azide.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
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- Antigène
- Fukutin (FKTN)
- Autre désignation
- FKTN (FKTN Produits)
- Synonymes
- anticorps FCMD, anticorps fcmd, anticorps im:7163166, anticorps zgc:162828, anticorps FKTN, anticorps CMD1X, anticorps LGMD2M, anticorps MDDGA4, anticorps MDDGB4, anticorps MDDGC4, anticorps D830030O17Rik, anticorps Fcmd, anticorps fukutin, anticorps fukutin S homeolog, anticorps Fukutin, anticorps FKTN, anticorps fktn, anticorps fktn.S, anticorps Bm1_09375, anticorps Bm1_09380, anticorps Bm1_44655, anticorps Fktn
- Sujet
- 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). Alternatively spliced transcript variants have been found for this gene.
- Poids moléculaire
- 54 kDa
- ID gène
- 2218
- UniProt
- O75072
- Pathways
- Regulation of Carbohydrate Metabolic Process
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