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Von Hippel-Lindau Tumor Suppressor, E3 Ubiquitin Protein Ligase (VHL) ELISA Kits

Von Hippel-Lindau syndrome (VHL) is a dominantly inherited familial cancer syndrome predisposing to a variety of malignant and benign tumors. Additionally we are shipping VHL Antibodies (112) and VHL Proteins (7) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
VHL 22346 P40338
VHL 7428 P40337
VHL 24874 Q64259
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Top VHL ELISA Kits at antibodies-online.com

Showing 4 out of 8 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Rat 0.113 ng/mL 0.31-20 ng/mL 96 Tests Log in to see 9 to 11 Days
$800.00
Details
Human
  96 Tests Log in to see 21 to 31 Days
$755.70
Details
Mouse
  96 Tests Log in to see 11 to 13 Days
$875.60
Details
Dog
  96 Tests Log in to see 11 to 13 Days
$1,095.60
Details

More ELISA Kits for VHL Interaction Partners

Mouse (Murine) Von Hippel-Lindau Tumor Suppressor, E3 Ubiquitin Protein Ligase (VHL) interaction partners

  1. Loss of Vhl in mesenchymal progenitors of the limb bud caused severe fibrosis of the synovial joints and formation of aggressive masses with histologic features of mesenchymal tumors.

  2. These data suggested that intestinal epithelial cells were injured after IM treatment through the pVHL overexpression-induced degradation of collagen I or HIF-1alpha (show HIF1A ELISA Kits).

  3. Vhl and Kif3a (show KIF3A ELISA Kits) deletion accelerates renal cyst formation

  4. maintains the stability and suppressive function of Foxp3 (show FOXP3 ELISA Kits)+ T cells via regulation of HIF-1a (show HIF1A ELISA Kits) pathway

  5. Deletion of the Vhl gene causes sympathoadrenal cell death and impairs chemoreceptor-mediated adaptation to hypoxia.

  6. Molecular dynamics of hif-1alpha (show HIF1A ELISA Kits) and VHL may determine the success of antineoplastic strategies in hypoxia-reoxygenation as predicted by computational modeling.

  7. Loss of Vhl in adult joint cartilage is associated with earlier dysregulation of cartilage homeostasis, characterized by increased chondrocyte apoptosis, compromised chondrocyte autophagy and accelerated age-related and surgery-induced OA development.

  8. Both Vhl and Bap1 (show BAP1 ELISA Kits) are required for kidney function. Even when Vhl is inactivated in multipotent nephron progenitor cells, Vhl loss is insufficient for renal tumorigenesis.

  9. VHL deficiency perturbs pancreas endocrine homeostasis in mice.

  10. data suggest that the VHL-mediated signaling in osteochondral progenitor cells plays a critical role in bone remodeling at postnatal/adult stages through coupling osteogenesis and angiogenesis

Human Von Hippel-Lindau Tumor Suppressor, E3 Ubiquitin Protein Ligase (VHL) interaction partners

  1. The VHL short variant is involved in protein quality control during translation.

  2. Study identified VHL as a direct target of miR (show MLXIP ELISA Kits)-101 and demonstrated that miR (show MLXIP ELISA Kits)-101 could increase HIF1alpha (show HIF1A ELISA Kits) protein levels by repressing VHL in normoxia condition.

  3. VHL inactivation is associated with gastrointestinal stromal tumors.

  4. indicate that HIF-1alpha (show HIF1A ELISA Kits)/pVHL/Hsp90 (show HSP90 ELISA Kits) interactions may be implicated in biology of different types of brain tumors through different signaling mechanisms

  5. misfolded TDP-43 (show TARDBP ELISA Kits) is cleared by VHL/CUL2 (show CUL2 ELISA Kits) in a step-wise manner via fragmentation.

  6. Overexpression of VHL is associated with multiple myeloma.

  7. HBV induces the HIF2alpha (show EPAS1 ELISA Kits) expression through its encoded protein HBx. This upregulates the HIF-2alpha (show EPAS1 ELISA Kits) expression by binding to the pVHL activating the NF-kappaB (show NFKB1 ELISA Kits) signaling pathway

  8. inhibition of miR566 expression increases the expression levels of VHL, decreases the expression levels of VEGF, and inhibits the invasive and migratory abilities of glioblastoma.

  9. proteome and phospho-proteomic analysis of isogenic 786-O renal cell carcinoma (+/-VHL) cells to compare signatures that reflect hypoxia and/or loss of VHL protein

  10. Pars (show EPRS ELISA Kits) plana vitrectomy in advanced VHL eye disease can improve or preserve visual function, but postoperative progression of ocular VHL disease can be accelerated in cases where retinotomy is performed.

VHL Antigen Profile

Antigen Summary

Von Hippel-Lindau syndrome (VHL) is a dominantly inherited familial cancer syndrome predisposing to a variety of malignant and benign tumors. A germline mutation of this gene is the basis of familial inheritance of VHL syndrome. The protein encoded by this gene is a component of the protein complex that includes elongin B, elongin C, and cullin-2, and possesses ubiquitin ligase E3 activity. This protein is involved in the ubiquitination and degradation of hypoxia-inducible-factor (HIF), which is a transcription factor that plays a central role in the regulation of gene expression by oxygen. RNA polymerase II subunit POLR2G/RPB7 is also reported to be a target of this protein. Alternatively spliced transcript variants encoding distinct isoforms have been observed.

Gene names and symbols associated with VHL

  • von Hippel-Lindau tumor suppressor (Vhl) antibody
  • von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase (VHL) antibody
  • von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase (Vhl) antibody
  • HRCA1 antibody
  • pVHL antibody
  • RCA1 antibody
  • VHL1 antibody
  • Vhlh antibody

Protein level used designations for VHL

pVHL , von Hippel-Lindau disease tumor suppressor , von Hippel-Lindau syndrome homolog , von Hippel-Lindau syndrome protein homolog , elongin binding protein , protein G7

GENE ID SPECIES
22346 Mus musculus
7428 Homo sapiens
24874 Rattus norvegicus
494000 Canis lupus familiaris
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