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Product Name ZNF132 Chinese Name Zinc finger protein132抗体 Alias pHZ 12; Zinc finger protein 132 (clone pHZ 12); Zinc finger protein 132 (clone pHZ12); Zinc finger protein 132; ZN132_HUMAN; ZNF132. literatures Specific References (2) | SL7150R has been referenced in 2 publications.[IF=3.15] Zhao Liu. et al. Downregulated ZNF132 predicts unfavorable outcomes in breast Cancer via Hypermethylation modification. Bmc Cancer. 2021 Dec;21(1):1-12 WB,IHC ; Human.[IF=2.933] Liu Z et al. Downregulated ZNF132 Predicts Unfavorable Outcomes in Breast Cancer via Hypermethylation Modification. BMC Cancer.2019. IHC ; Human.Research Area transcriptional regulatory factor Zinc finger protein Epigenetics Immunogen Species Rabbit Clonality Polyclonal React Species (predicted: Human, ) Applications WB=1:500-2000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.Theoretical molecular weight 81kDa Cellular localization The nucleus Form Liquid Concentration 1mg/ml immunogen KLH conjugated synthetic peptide derived from human ZNF132: 121-220/706 Lsotype IgG Purification affinity purified by Protein A Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. PubMed PubMed Product Detail ZNF132 (Zinc Finger Protein 132) is a Protein Coding gene. GO annotations related to this gene include nucleic acid binding and transcription factor activity, sequence-specific DNA binding. An important paralog of this gene is ZNF304.
Function:
May be involved in transcriptional regulation.
Subcellular Location:
Nucleus.
Similarity:
Belongs to the krueppel C2H2-type zinc-finger protein family.
Contains 18 C2H2-type zinc fingers.
Contains 1 KRAB domain.
SWISS:
P52740
Gene ID:
7691
Database links:Entrez Gene: 7691 Human
Omim: 604074 Human
SwissProt: P52740 Human
Unigene: 156169 Human
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