Anti-TCEB2 antibody [R76-4B-1] (STJA0035599)

SPECIFICATIONS
ClonalityMonoclonal
HostRabbit
ConjugationUnconjugated
IsotypeIgG
ImmunogenA synthesized peptide derived from human TCEB2
STJA0035599
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General Information

Short DescriptionRabbit monoclonal anti-TCEB2 for use in WB in Human samples. Datasheet included with dilution recommendations, and related reagents.
ApplicationsWB
HostRabbit
ReactivityHuman
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

ClonalityMonoclonal
Clone IDR76-4B-1
IsotypeIgG
ConjugationUnconjugated
PurificationAffinity Chromatography
Dilution RangeWB 1:500-1:1000
FormulationLiquid in PBS, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Storage InstructionStore at 4°C short term. Aliquot and store at-20°C long term. Avoid freeze/thaw cycles.

Target Information

Gene SymbolELOB
Gene ID6923
Uniprot IDELOB_HUMAN
ImmunogenA synthesized peptide derived from human TCEB2

Additional Info

Function SIII, also known as elongin, is a general transcription elongation factor that increases the RNA polymerase II transcription elongation past template-encoded arresting sites. Subunit A is transcriptionally active and its transcription activity is strongly enhanced by binding to the dimeric complex of the SIII regulatory subunits B and C (elongin BC complex). In embryonic stem cells, the elongin BC complex is recruited by EPOP to Polycomb group (PcG) target genes in order generate genomic region that display both active and repressive chromatin properties, an important feature of pluripotent stem cells. Core component of multiple cullin-2 and cullin-5-RING E3 ubiquitin-protein ligase complexes (ECS complexes), which mediate the ubiquitination of target proteins. By binding to BC-box motifs it seems to link target recruitment subunits, like VHL and members of the SOCS box family, to Cullin/RBX1 modules that activate E2 ubiquitination enzymes. Component the von Hippel-Lindau ubiquitination complex CBC(VHL). A number of ECS complexes (containing either KLHDC2, KLHDC3, KLHDC10, APPBP2, FEM1A, FEM1B or FEM1C as substrate-recognition component) are part of the DesCEND (destruction via C-end degrons) pathway, which recognizes a C-degron located at the extreme C terminus of target proteins, leading to their ubiquitination and degradation. The ECS(ASB9) complex mediates ubiquitination and degradation of CKB. As part of a multisubunit ubiquitin ligase complex, polyubiquitinates monoubiquitinated POLR2A. ECS(LRR1) ubiquitinates MCM7 and promotes CMG replisome disassembly by VCP and chromatin extraction during S-phase. As part of the ECS(RAB40C) complex, mediates ANKRD28 ubiquitination and degradation, thereby inhibiting protein phosphatase 6 (PP6) complex activity and focal adhesion assembly during cell migration. (Microbial infection) Following infection by HIV-1 virus, component of a cullin-5-RING E3 ubiquitin-protein ligase complex (ECS complex) hijacked by the HIV-1 Vif protein, which catalyzes ubiquitination and degradation of APOBEC3F and APOBEC3G. The complex can also ubiquitinate APOBEC3H to some extent.
Protein Name Elongin-B
Elob
Elongin 18 Kda Subunit
Rna Polymerase Ii Transcription Factor Siii Subunit B
Siii P18
Transcription Elongation Factor B Polypeptide 2
Database Links Reactome: R-HSA-112382
Reactome: R-HSA-1234176
Reactome: R-HSA-167152
Reactome: R-HSA-167200
Reactome: R-HSA-167238
Reactome: R-HSA-167243
Reactome: R-HSA-167246
Reactome: R-HSA-167287
Reactome: R-HSA-167290
Reactome: R-HSA-180585
Reactome: R-HSA-674695
Reactome: R-HSA-6796648
Reactome: R-HSA-75955
Reactome: R-HSA-8951664
Reactome: R-HSA-9010553
Reactome: R-HSA-9705462
Reactome: R-HSA-983168
Reactome: R-HSA-9833109
Cellular Localisation Nucleus
Alternative Antibody Names Anti-Elongin-B antibody
Anti-Elob antibody
Anti-Elongin 18 Kda Subunit antibody
Anti-Rna Polymerase Ii Transcription Factor Siii Subunit B antibody
Anti-Siii P18 antibody
Anti-Transcription Elongation Factor B Polypeptide 2 antibody
Anti-ELOB antibody
Anti-TCEB2 antibody

Information sourced from Uniprot.org

Citations

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