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THAP1 Rabbit pAb

THAP1 Rabbit pAb

     
  • 1 - THAP1 Rabbit pAb AP58595
    Sample:
    Lane 1: Mouse Muscle tissue lysates
    Lane 2: Mouse Kidney tissue lysates
    Lane 3: Mouse Liver tissue lysates
    Lane 4: Mouse Thymus tissue lysates
    Lane 5: Rat Heart tissue lysates
    Lane 6: Rat Muscle tissue lysates
    Lane 7: Rat Kidney tissue lysates
    Lane 8: Rat Liver tissue lysates
    Lane 9: Rat Thymus tissue lysates
    Lane 10: Human Molt-4 cell lysates
    Lane 11: Human Huvec cell lysates
    Lane 12: Human U251 cell lysates
    Primary: Anti-THAP1 (AP58595) at 1/1000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 25 kD
    Observed band size: 27 kD
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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
Primary Accession Q9NVV9
Reactivity Human, Mouse, Rat
Predicted Chicken, Dog, Rabbit, Sheep
Host Rabbit
Clonality Polyclonal
Calculated MW 24944 Da
Physical State Liquid
Immunogen KLH conjugated synthetic peptide derived from human THAP1
Epitope Specificity 121-213/213
Purity affinity purified by Protein A
Buffer 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
SUBCELLULAR LOCATION Nucleus, nucleoplasm. Nucleus, PML body.
SIMILARITY Belongs to the THAP1 family. Contains 1 THAP-type zinc finger.
SUBUNIT Interacts with PAWR. Component of a THAP1/THAP3-HCFC1-OGT complex that contains, either THAP1 or THAP3, HCFC1 and OGT. Interacts with OGT. Interacts (via the HBM) with HCFC1 (via the Kelch-repeat domain); the interaction recruits HCFC1 to the RRM1 promoter.
DISEASE Defects in THAP1 are the cause of dystonia type 6 (DYT6) [MIM:602629]. DYT6 is a primary torsion dystonia. Dystonia is defined by the presence of sustained involuntary muscle contractions, often leading to abnormal postures. Dystonia type 6 is characterized by onset in early adulthood, cranial or cervical involvement in about half of the cases, and frequent progression to involve multiple body regions.
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
Background Descriptions THAP1 contains a THAP domain, a zinc-dependent DNA-binding domain. It colocalizes with the apoptosis response protein PAWR/PAR-4 in promyelocytic leukemia (PML) nuclear bodies and is a pro-apoptopic protein that potentiates both serum-withdrawal and TNF-induced apoptosis. It is a physiologic regulator of endothelial cell proliferation and cell-cycle progression, two essential processes for angiogenesis.
Additional Information
Gene ID 55145
Other Names THAP domain-containing protein 1, THAP1
Target/Specificity Highly expressed in heart, skeletal muscle, kidney and liver. Weaker expression in brain and placenta.
Dilution WB=1:500-2000
StorageStore at -20 °C for one year. Avoid repeated freeze/thaw cycles. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Protein Information
Name THAP1
Function DNA-binding transcription regulator that regulates endothelial cell proliferation and G1/S cell-cycle progression. Specifically binds the 5'-[AT]NTNN[GT]GGCA[AGT]-3' core DNA sequence and acts by modulating expression of pRB-E2F cell-cycle target genes, including RRM1. Component of a THAP1/THAP3-HCFC1-OGT complex that is required for the regulation of the transcriptional activity of RRM1. May also have pro-apoptotic activity by potentiating both serum- withdrawal and TNF-induced apoptosis.
Cellular Location Nucleus, nucleoplasm. Nucleus, PML body
Tissue Location Highly expressed in heart, skeletal muscle, kidney and liver. Weaker expression in brain and placenta
Research Areas

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

BACKGROUND

THAP1 contains a THAP domain, a zinc-dependent DNA-binding domain. It colocalizes with the apoptosis response protein PAWR/PAR-4 in promyelocytic leukemia (PML) nuclear bodies and is a pro-apoptopic protein that potentiates both serum-withdrawal and TNF-induced apoptosis. It is a physiologic regulator of endothelial cell proliferation and cell-cycle progression, two essential processes for angiogenesis.

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