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Human Monoclonal WHSC2 Primary Antibody for ICC, FACS - ABIN1724801
Yung, Narita, Komori, Yamaguchi, Handa: Cellular dynamics of the negative transcription elongation factor NELF. in Experimental cell research 2009
Show all 2 Pubmed References
Human Monoclonal WHSC2 Primary Antibody for ICC, FACS - ABIN1724802
Kerzendorfer, Hannes, Colnaghi, Abramowicz, Carpenter, Vermeesch, ODriscoll: Characterizing the functional consequences of haploinsufficiency of NELF-A (WHSC2) and SLBP identifies novel cellular phenotypes in Wolf-Hirschhorn syndrome. in Human molecular genetics 2012
Show all 2 Pubmed References
The finding that both phenotypes of arrested embryos are obtained in embryos that lack maternally provided NELF-A as well as in embryos with reduced levels of maternal NELF-E show that these phenotypes result from the reduced activity of the NELF complex.
analysis of the interactions between DSIF (show SUPT4H1 Antibodies) (DRB sensitivity inducing factor), NELF (negative elongation factor (show RDBP Antibodies)), and the Drosophila RNA polymerase II transcription elongation complex
A positively charged face of NELF-AC is involved in RNA binding, whereas the opposite face of the NELF-AC subcomplex binds NELF-B (show COBRA1 Antibodies). NELF-B (show COBRA1 Antibodies) is predicted to form a HEAT repeat fold, also binds RNA in vivo, and anchors the subunit NELF-E (show RDBP Antibodies), which is confirmed to bind RNA in vivo.
These studies allow us to position the actions of two new modulators of GR-regulated transactivation, NELF-A and NELF-B (show COBRA1 Antibodies), relative to other factors in the overall gene induction sequence.
data show that NELF subunits exhibit highly specific subcellular localizations, such as in NELF bodies or in midbodies, and some shuttle actively between the nucleus and cytoplasm; loss of NELF from cells can lead to enlarged and/or multiple nuclei
haploinsufficiency of SLBP (show SLBP Antibodies) and/or WHSC2 (NELF-A) contributes to several novel cellular phenotypes of WHS (show WHSC1 Antibodies).
NELF-C (show TH1L Antibodies) and NELF-D (show TH1L Antibodies) are highly related or identical to the protein called TH1 (show TH1L Antibodies), of unknown function. NELF-B (show COBRA1 Antibodies) and NELF-C (show TH1L Antibodies) or NELF-D (show TH1L Antibodies) are integral subunits that bring NELF-A and NELF-E (show RDBP Antibodies) together. [NELF-B (show COBRA1 Antibodies)] [NELF-C (show TH1L Antibodies)]
connection between the syndrome phenotype and cytogenetic abnormalities, through gradual shortening of the length of the critical region WHSCR (finally up to 165 kb), and sequencing it, at least 2 genes (WHSC1 (show WHSC1 Antibodies) and WHSC2) were identified.
Negative elongation factor (NELF (show RDBP Antibodies)) is a four subunit transcription factor. Our results point to a surprising role of NELF in the 3' end processing of histone mRNAs and suggest that NELF is a new factor that coordinates mRNA processing in transcription
This gene is expressed ubiquitously with higher levels in fetal than in adult tissues. It encodes a protein sharing 93% sequence identity with the mouse protein. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene is mapped to the 165 kb WHS critical region, and may play a role in the phenotype of the WHS or Pitt-Rogers-Danks syndrome. The encoded protein is found to be capable of reacting with HLA-A2-restricted and tumor-specific cytotoxic T lymphocytes, suggesting a target for use in specific immunotherapy for a large number of cancer patients. This protein has also been shown to be a member of the NELF (negative elongation factor) protein complex that participates in the regulation of RNA polymerase II transcription elongation.
, negative elongation factor A
, Wolf-Hirschhorn syndrome candidate 2 protein
, Wolf-Hirschhorn syndrome candidate 2
, negative elongation factor A-like
, wolf-Hirschhorn syndrome candidate 2 protein
, Wolf-Hirschhorn syndrome candidate 2 homolog