GTX81135
MPZ antibody, C-term
Eine Lieferung in diese Region ist nicht möglich.
- SKU:
- GTX81135
- Zusätzliche Namen:
- myelin protein zero , CHM , CHN2 , CMT1 , CMT1B , CMT2I , CMT2J , CMT4E , CMTDI3 , CMTDID , DSS , HMSNIB , MPP , P0
- Anwendung:
- Flow Cytometry, WB, IHC-P
- Physischer Zustand:
- Liquid
- Spezies-Reaktivität:
- Human
- Aufreinigung:
- Affinity Purified; 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, 0.09% Sodium azide.
- Immunogen:
- KLH conjugated synthetic peptide between 186-215 amino acids from the C-terminal region of human MPZ.
- Uniprot:
- P25189
- Synonyme:
- Charcot-Marie-Tooth neuropathy 1B;CHM;CHN2;CMT1;CMT1B;CMT2I;CMT2J;CMT4E;CMTDI3;CMTDID;DSS;HMSNIB;MPP;myelin peripheral protein;myelin protein P0;Myelin protein zero;P0
- Weitere Details:
- This gene is specifically expressed in Schwann cells of the peripheral nervous system and encodes a type I transmembrane glycoprotein that is a major structural protein of the peripheral myelin sheath. The encoded protein contains a large hydrophobic extracellular domain and a smaller basic intracellular domain, which are essential for the formation and stabilization of the multilamellar structure of the compact myelin. Mutations in this gene are associated with autosomal dominant form of Charcot-Marie-Tooth disease type 1 (CMT1B) and other polyneuropathies, such as Dejerine-Sottas syndrome (DSS) and congenital hypomyelinating neuropathy (CHN). A recent study showed that two isoforms are produced from the same mRNA by use of alternative in-frame translation termination codons via a stop codon readthrough mechanism. [provided by RefSeq, Oct 2015]
- Versandbedingungen:
- Blue Ice