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Anti-MAX Rabbit mAb [96K19F99]

Purified Recombinant Rabbit Monoclonal Antibody

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货号 规格 价格
R015554
20µL ¥588.00
50µL ¥1080.00
100µL ¥1780.00

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Anti-MAX Rabbit mAb [96K19F99]
Anti-MAX Rabbit mAb [96K19F99]
Anti-MAX Rabbit mAb [96K19F99]
Product NameAnti-MAX Rabbit mAb
DescriptionPurified Recombinant Rabbit Monoclonal Antibody
Application
  • Applications Legend:
  • WB=Western Blotting
  • IHC-P=Immunohistochemistry (Paraffin)
  • IHC-F=Immunohistochemistry (Frozen)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IHC-P/IF (Tissue-P), ELISA
DilutionWB 1:1,000~1:2,000; IHC-P 1:100~1:200; IF 1:100~1:200
ReactivityHuman, Mouse, Rat
HostRabbit
ClonalityMonoclonal
Clone No.96K19F99
IsotypeIgG
LabelUnconjugated
ImmunogenRecombinant protein of human MAX
FormatAffinity purified monoclonal antibody supplied in PBS with 0.01% sodium azide and 50% glycerol, pH 7.3.
SynonymsbHLHd4; bHLHd5; bHLHd6; bHLHd7; bHLHd8; Class D basic helix-loop-helix protein 4; Helix loop helix zipper protein; Max; MAX protein; MAX_HUMAN; MGC10775; MGC11225; MGC18164; MGC34679; MGC36767; MYC associated factor X; Myc binding novel HLH/LZ protein; Myc-associated factor X; Orf 1; Orf1; Protein max.
Molecular weightCalculated MW: 18 kDa; Observed MW: 18 kDa
Uniprot ID P61244 , P28574 , P52164
Gene ID 4149 , 17187 , 60661
StorageShipped on wet ice. Store at -20℃. Stable for 24 months from date of receipt. Aliquoting is unnecessary for -20℃ storage.
PrecautionsAnti-MAX Rabbit mAb [96K19F99] is for research use only and not for use in diagnostic or therapeutic procedures.
Background The protein encoded by this gene is a member of the basic helix-loop-helix leucine zipper (bHLHZ) family of transcription factors. It is able to form homodimers and heterodimers with other family members, which include Mad, Mxi1 and Myc. Myc is an oncoprotein implicated in cell proliferation, differentiation and apoptosis. The homodimers and heterodimers compete for a common DNA target site (the E box) and rearrangement among these dimer forms provides a complex system of transcriptional regulation. Mutations of this gene have been reported to be associated with hereditary pheochromocytoma. A pseudogene of this gene is located on the long arm of chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]
Cellular Location Nucleus. Cell projection, dendrite.
Tissue Location High levels found in the brain, heart and lung while lower levels are seen in the liver, kidney and skeletal muscle.

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