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ZNF287 Antibody (N-term)

Affinity Purified Rabbit Polyclonal Antibody (Pab)

     
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  • 1 - ZNF287 Antibody (N-term) AP18286a
    ZNF287 Antibody (N-term) (Cat. #AP18286a) western blot analysis in A549 cell line lysates (35ug/lane).This demonstrates the ZNF287 antibody detected the ZNF287 protein (arrow).
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, E
Primary Accession Q9HBT7
Other Accession NP_065704.2
Reactivity Human
Host Rabbit
Clonality Polyclonal
Isotype Rabbit IgG
Calculated MW 88339 Da
Antigen Region 124-150 aa
Additional Information
Gene ID 57336
Other Names Zinc finger protein 287, Zinc finger protein with KRAB and SCAN domains 13, ZNF287, ZKSCAN13
Target/Specificity This ZNF287 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 124-150 amino acids from the N-terminal region of human ZNF287.
Dilution WB~~1:1000
E~~Use at an assay dependent concentration.
Format Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsZNF287 Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name ZNF287 (HGNC:13502)
Synonyms ZKSCAN13
Function May be involved in transcriptional regulation.
Cellular Location Nucleus.
Research Areas

For Research Use Only. Not For Use In Diagnostic Procedures.

BACKGROUND

This gene encodes a member of the krueppel family of zinc finger proteins, suggesting a role as a transcription factor. Its specific function has not been determined. This gene is located near the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq].

REFERENCES

Dang, D.T., et al. Int. J. Biochem. Cell Biol. 32 (11-12), 1103-1121 (2000) :
Leon, O., et al. Biol. Res. 33(1):21-30(2000)

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