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![Fukutin antibody [N3C3-2]](https://www.genetex.com/upload/website/prouct_img/normal/GTX110302/GTX110302_WB_w_23060500_761.webp)
GTX110302
Fukutin antibody [N3C3-2]
Eine Lieferung in diese Region ist nicht möglich.
- SKU:
- GTX110302
- Zusätzliche Namen:
- fukutin , CMD1X , FCMD , LGMD2M , LGMDR13 , MDDGA4 , MDDGB4 , MDDGC4
- Anwendung:
- WB, IHC-P, IF, ICC
- Konzentration:
- 1 mg/ml
- Physischer Zustand:
- Liquid
- Spezies-Reaktivität:
- Human
- Aufreinigung:
- Affinity Purified
- Lagerbedingungen:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Hersteller:
- Genetex
- Host:
- Rabbit
- Reaktivitäten:
- Human
- Buffer:
- 0.1M Tris, 0.1M Glycine, 10% Glycerol, 0.01% Thimerosal.
- Immunogen:
- Recombinant protein encompassing a sequence within the center region of human Fukutin. The exact sequence is proprietary.
- Klon:
- N3C3-2
- Uniprot:
- O75072
- Synonyme:
- CMD1X;FCMD;fukutin;Fukuyama type congenital muscular dystrophy protein;Fukuyama-type congenital muscular dystrophy protein;LGMD2M;LGMDR13;MDDGA4;MDDGB4;MDDGC4;patient fukutin;ribitol-5-phosphate transferase
- Weitere Details:
- 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]
- Versandbedingungen:
- Blue Ice