SIAH2 antibody

Principal name

SIAH2 antibody

Alternative names for SIAH2 antibody

Siah-2, E3 ubiquitin-protein ligase SIAH2, Seven in absentia homolog 2

SwissProt ID

O43255 (Human), Q06986 (Mouse), Q7SYL3 (Danre), Q8R4T2 (Rat), Q9I8X5 (Xenla)

Gene ID

6478 (SIAH2), 20439 (Siah2), 140593

Available reactivities

Hu (Human), Bov (Bovine), Chk (Chicken), Dros (Drosophila), Ms (Mouse), Rt (Rat), Ze (Zebrafish), African clawed frog, Can (Canine), Eq (Equine), GP (Guinea Pig), Rb (Rabbit), Por (Porcine)

Available hosts

Mouse, Rabbit

Available applications

Enzyme Immunoassay (E), Frozen Sections (C), Immunocytochemistry/Immunofluorescence (ICC/IF), Paraffin Sections (P), Flow Cytometry (F), Western blot / Immunoblot (WB)

Background of SIAH2 antibody

SIAH-2 (seven in absentia homolog 2) is an E3 ligase that catalyzes ubiquitination and proteasome-mediated degradation of protein substrates. SIAH-2 encodes a 324 amino acid protein that shares 77% identity with human SIAH-1 and 68% identity with the Drosophila sina (seven in absentia) gene, on which development of the Drosophila R7 photoreceptor is dependent. SIAH-2 targets TRAF2 (which regulates cell responses to stress and cytokines through the regulation of key stress-signaling cascades) for degradation under stress conditions such as hypoxia. It targets HIF-1alpha prolyl hydroxylase 3 (PHD3) for degradation upon exposure to hypoxic conditions, which coincides with an increase in SIAH-2 transcription. SIAH-2 can decrease TNF-alpha-dependent induction of JNK activity and transcriptional activation of NFkappaB. SIAH-2 null mice subjected to hypoxia display an impaired respiratory response and reduced levels of hemoglobin.

General readings

Fiucci G. et al. Siah-1b is a direct transcriptional target of p53: identification of the functional p53 responsive element in the siah-1b promoter.Proc Natl Acad Sci U S A. 2004;101(10):3510-5.

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Lysates

Catalog No.    

SIAH2 overexpression lysate

SIAH2 overexpression lysate  
0.1 mg / €295.00
  OriGene Technologies, Inc.

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