SKU: WP3678 Categories: ,

TRI37 rabbit pAb

Price range: $268.00 through $328.00

SKU: WP3678-100
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Product details

Background:

This gene encodes a member of the tripartite motif (TRIM) family, whose members are involved in diverse cellular functions such as developmental patterning and oncogenesis. The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain. The RING finger and B-box domains chelate zinc and might be involved in protein-protein and/or protein-nucleic acid interactions. The gene mutations are associated with mulibrey (muscle-liver-brain-eye) nanism, an autosomal recessive disorder that involves several tissues of mesodermal origin. [provided by RefSeq, Mar 2016],

Specifications

Size50μL/100μL
TargetTRI37
ReactivityHuman, Mouse
ApplicationsWB
MW(Calculated)
MW(Observed)105kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human TRI37 AA range: 315-365
SpecificityThis antibody detects endogenous levels of TRI37 at Human/Mouse
Gene NameTRIM37 KIAA0898 MUL POB1
Protein NameTRI37
Other NameE3 ubiquitin-protein ligase TRIM37; / Mulibrey nanism protein; / Tripartite motif-containing protein 37
SpeciesHuman
Gene ID4591
UniprotO94972,
Species.1Mouse
Gene ID.168729
Uniprot.1Q6PCX9
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationCytoplasm, perinuclear region . Peroxisome . Found in vesicles of the peroxisome. Aggregates as aggresomes, a perinuclear region where certain misfolded or aggregated proteins are sequestered for proteasomal degradation. .
Tissue ExpressionUbiquitous (PubMed:10888877). Highly expressed in testis, while it is weakly expressed in other tissues (PubMed:16310976).
Signaling_pathwayGenetic Information Processing >> Folding, sorting and degradation >> Ubiquitin mediated proteolysis
Research Areas>>Ubiquitin mediated proteolysis
FunctionDisease:Defects in TRIM37 are the cause of mulibrey nanism (MUL) [MIM:253250]; also called muscle-liver-brain-eye nanism. Mulibrey nanism is an autosomal recessive disorder that involves several tissues of mesodermal origin, implying a defect in a highly pleiotropic gene. Characteristic features include severe growth failure of prenatal onset and constrictive pericardium with consequent hepatomegaly. In addition, muscle hypotonia, J-shaped sella turcica, yellowish dots in the ocular fundi, typical dysmorphic features and hypoplasia of various endocrine glands causing hormonal deficiency are common.,similarity:Belongs to the TRIM/RBCC family.,similarity:Contains 1 B box-type zinc finger.,similarity:Contains 1 MATH domain.,similarity:Contains 1 RING-type zinc finger.,subcellular location:Found in vesicles of the peroxisome.,tissue specificity:Ubiquitous.,
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