您当前的位置：
PMP22 (DGR33988) Rabbit mAb
db13009
Datasheet
- Background This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Studies suggest two alternately used promoters drive tissue-specific expression. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
- Immunogen A synthetic peptide of human PMP22
-
Gene ID
5376
-
Swiss Prot
Q01453
- Synonyms DSS; CIDP; GAS3; HNPP; CMT1A; CMT1E; GAS-3; Sp110; HMSNIA
- Reactivity Human
- Application WB, IHC-P, ICC/IF, FC, IP
-
Recommended dilution
WB: 1:1000
IHC-P: 1:2000-1:20000
ICC/IF: 1:100-1:200
FC: 1:200-1:500
IP: 1:20-1:50 - Calculated MW 18 kDa
- Observed MW 22 kDa
- Host species Rabbit
- Clonality Monoclonal
- Clonality No. DGR33988
- Isotype IgG
- Purity Affinity Purification
- Conjugation Un-conjugated
- Storage/Stability Store at -20°C. Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.
订购信息
- Package Price (RMB)
- 10μL 398
- 20μL 698
- 50μL 1398
- 100μL 2398
- 货期：现货
相关产品
For research use only. Not intended for diagnostic.
