Comparison

TRIM74 Polyclonal Antibody

Item no. E-AB-17151-120
Manufacturer Elabscience
Amount 120uL
Category
Type Antibody Polyclonal
Applications IHC, ELISA
Specific against Human
Host Rabbit
Isotype IgG
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias MGC45440, TRI74, TRIM 74, TRIM74, Tripartite motif containing 50C, Tripartite motif containing 74, Tripartite motif containing protein 50C, Tripartite motif containing protein 74, Tripartite motif-containing protein 50C, Tripartite motif-containing protei
Similar products TRIM74, Tripartite motif-containing protein 74, Tripartite motif-containing protein 50C, MGC45440, TRI74, TRIM 74, Tripartite motif containing 50C, Tripartite motif containing 74, Tripartite motif containing protein 50C, Tripartite motif containing protein 74
Available
Research Areas
Epigenetics and Nuclear Signaling
Synonyms
MGC45440, TRI74, TRIM 74, TRIM74, Tripartite motif containing 50C, Tripartite motif containing 74, Tripartite motif containing protein 50C, Tripartite motif containing protein 74, Tripartite motif-containing protein 50C, Tripartite motif-containing protein 74
Swissprot
Q86UV6
Background
TRIM 74 (Tripartite motif-containing protein 74) is a possible protein coding regions found at gene location 7q11.23. Tripartite motif (TRIM) proteins play important roles in a variety of cellular functions including cell proliferation, differentiation, development, oncogenesis, and apoptosis. TRIM gene expression analysis in primary human immune cells seem to suggest the involvement of TRIM proteins in also regulating host antiviral activities. The gene encoding TRIM 74 maps to human chromosome 7, which houses over 1, 000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
Concentration
1.1 mg/mL
Storage
Store at -20C. Avoid freeze / thaw cycles.
Immunogen
Full length fusion protein
Buffer
PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification Method
Affinity purification
Dilution
IHC 1:30-150, ELISA 1:2000-10000
Conjugation
Unconjugated
Gene Accession
BC033871

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 120uL
Available: In stock
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