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Meckelin (DGR32600) Rabbit mAb
db12492
Datasheet
- Background The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6). [provided by RefSeq, Nov 2008]
- Immunogen A synthetic peptide of human Meckelin
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Gene ID
91147
-
Swiss Prot
Q5HYA8
- Synonyms MKS3; JBTS6; NPHP11; TNEM67; MECKELIN
- Reactivity Human,Mouse,Rat
- Application WB, IHC-P, ICC/IF, FC
-
Recommended dilution
WB: 1:1000
IHC-P: 1:100-1:200
ICC/IF: 1:500-1:1000
FC: 1:200-1:500 - Calculated MW 112 kDa
- Observed MW 112 kDa
- Host species Rabbit
- Clonality Monoclonal
- Clonality No. DGR32600
- 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 Meckelin in Hela,A549,HL-60,U251,U87-MG cell lysates using Meckelin antibody(1:1000 diluted). -
Immunofluorescent analysis of MCF-7 cells using db12492 antibody (green), and DAPI (blue).
订购信息
- Package Price (RMB)
- 10μL 398
- 20μL 698
- 50μL 1398
- 100μL 2398
- 货期：现货
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For research use only. Not intended for diagnostic.
