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Conjugation/Formulation：Un-conjugated
- Background This gene encodes a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS). CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014]
- Immunogen A synthetic peptide of human ERCC8
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Gene ID
1161
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Swiss Prot
Q13216
- Synonyms CSA; CKN1; UVSS2
- Reactivity Human
- Application WB, IP
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Recommended dilution
WB: 1:1000-1:5000
IP: 1:10-1:100 - Calculated MW 44 kDa
- Observed MW 44 kDa
- Host species Rabbit
- Clonality Monoclonal
- Clonality No. DGR31369
- 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.
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Western blot detection of ERCC8 in A549,HL-60,U251,U87-MG cell lysates using ERCC8 antibody(1:1000 diluted).
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.
