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NHLRC1/Malin Rabbit mAb (A26247)

Datasheet

Tested applications:WBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibitionReactivity:Human

ABclonal:Western blot - NHLRC1/Malin Rabbit mAb (A26247)

Western blot analysis of lysates from wild type (WT) and 293T cells transfected with NHLRC1/Malin using NHLRC1/Malin Rabbit mAb (A26247) at 1:9000 dilution incubated overnight at 4℃.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 20 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020)
.Exposure time: 15s.

ABclonal:Immunofluorescence - NHLRC1/Malin Rabbit mAb (A26247)

Confocal imaging of A549 cells using NHLRC1/Malin Rabbit mAb (A26247, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). The cells were counterstained with α-tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (AS076, dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.

Overview

Product nameNHLRC1/Malin Rabbit mAb
Catalog No.A26247
Host speciesRabbit
Purification methodAffinity purification
IsotypeIgG
CloneNo.ARC68981
The protein encoded by this gene is a single subunit E3 ubiquitin ligase. Laforin is polyubiquitinated by the encoded protein. Defects in this intronless gene lead to an accumulation of laforin and onset of Lafora disease, also known as progressive myoclonic epilepsy type 2 (EPM2).
ImmunogenRecombinant fusion protein containing a sequence corresponding to amino acids 79-280 of human NHLRC1 (NP_940988.2).
SequenceDTSDCLPVLHLIELLGSALRQSPAAHRAAPSAPGALTCHHTFGGWGTLVNPTGLALCPKTGRVVVVHDGRRRVKIFDSGGGCAHQFGEKGDAAQDIRYPVDVTITNDCHVVVTDAGDRSIKVFDFFGQIKLVIGGQFSLPWGVETTPQNGIVVTDAEAGSLHLLDVDFAEGVLRRTERLQAHLCNPRGVAVSWLTGAIAVLE
Gene ID
Swiss Prot
SynonymsEPM2A; EPM2B; MALIN; bA204B7.2
Calculated MW42kDa
Observed MW50kDa
ReactivityHuman
Tested applicationsWBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibition
Recommended dilution
  • WB 1:2000 - 1:10000
  • IF/ICC 1:50 - 1:200
  • ELISA Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
Storage bufferStore at -20℃. Avoid freeze / thaw cycles.
Buffer: PBS with 0.09% Sodium azide, 0.05% BSA, 50% glycerol, pH7.3.
Key applicationWestern blotting    Immunofluorescence    
Positive samples293T
Cellular locationEndoplasmic reticulum, Nucleus.

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ABclonal:Western blot - NHLRC1/Malin Rabbit mAb (A26247)}

Western blot - NHLRC1/Malin Rabbit mAb (A26247)

Western blot analysis of lysates from wild type (WT) and 293T cells transfected with NHLRC1/Malin using NHLRC1/Malin Rabbit mAb (A26247) at 1:9000 dilution incubated overnight at 4℃.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 20 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020)
.Exposure time: 15s.
ABclonal:Immunofluorescence - NHLRC1/Malin Rabbit mAb (A26247)}

Immunofluorescence - NHLRC1/Malin Rabbit mAb (A26247)

Confocal imaging of A549 cells using NHLRC1/Malin Rabbit mAb (A26247, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). The cells were counterstained with α-tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (AS076, dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.

* For research use only. Not for therapeutic or diagnostic purposes.

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