![Fibrillin 1 antibody [C3], C-term](https://www.genetex.com/upload/website/prouct_img/normal/GTX101216/GTX101216_WB_w_23060100_376.webp)
GTX101216
Fibrillin 1 antibody [C3], C-term
Eine Lieferung in diese Region ist nicht möglich.
- SKU:
- GTX101216
- Zusätzliche Namen:
- fibrillin 1 , ACMICD , ECTOL1 , FBN , GPHYSD2 , MASS , MFLS , MFS1 , OCTD , SGS , SSKS , WMS , WMS2
- Anwendung:
- WB
- Konzentration:
- 2 mg/ml
- Physischer Zustand:
- Liquid
- Spezies-Reaktivität:
- Human
- Aufreinigung:
- Protein A 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:
- PBS, 40% Glycerol, 0.01% Thimerosal.
- Immunogen:
- Recombinant protein encompassing a sequence within the C-terminus region of human Fibrillin 1. The exact sequence is proprietary.
- Klon:
- C3
- Uniprot:
- P35555
- Synonyme:
- ACMICD;asprosin;ECTOL1;epididymis secretory sperm binding protein;FBN;fibrillin 15;fibrillin-1;fibrillin-1 preproprotein;GPHYSD2;MASS;MFLS;MFS1;OCTD;SGS;SSKS;WMS;WMS2
- Weitere Details:
- This gene encodes a member of the fibrillin family. The encoded protein is a large, extracellular matrix glycoprotein that serve as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body. Mutations in this gene are associated with Marfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome. [provided by RefSeq]
- Versandbedingungen:
- Blue Ice