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ZNF674 Antibody (N-term)

Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)

     
  • 1 - ZNF674 Antibody (N-term) AP10912a
    ZNF674 Antibody (N-term) (Cat. #AP10912a) western blot analysis in CEM cell line lysates (35ug/lane).This demonstrates the ZNF674 antibody detected the ZNF674 protein (arrow).
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Product info
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 Q2M3X9
Other Accession Q5JUW0, NP_001034980.1
Reactivity Human
Host Rabbit
Clonality Polyclonal
Isotype Rabbit Ig
Calculated MW 67199 Da
Additional info
Gene ID 641339
Other Names Zinc finger protein 674, ZNF674
Target/Specificity This ZNF674 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 74-102 amino acids from the N-terminal region of human ZNF674.
Dilution WB~~1:1000
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.
PrecautionsZNF674 Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name ZNF674
Function May be involved in transcriptional regulation.
Cellular Location Nucleus.
Tissue Location Expressed in testis.
Research Areas

BACKGROUND

This gene encodes a zinc finger protein with an N-terminal Kruppel-associated box-containing (KRAB) domain and 11 Kruppel-type C2H2 zinc finger domains. Like other zinc finger proteins, this gene may function as a transcription factor. This gene resides on an area of chromosome X that has been implicated in nonsyndromic X-linked mental retardation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq].

REFERENCES

Lugtenberg, D., et al. Am. J. Hum. Genet. 78(2):265-278(2006)
Venter, J.C., et al. Science 291(5507):1304-1351(2001)

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