TRIP4 antibody
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- Target See all TRIP4 Antibodies
- TRIP4 (Thyroid Hormone Receptor Interactor 4 (TRIP4))
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Reactivity
- Human, Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This TRIP4 antibody is un-conjugated
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Application
- Western Blotting (WB), Immunohistochemistry (IHC)
- Characteristics
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogen
- Recombinant human Activating signal cointegrator 1 protein
- Isotype
- IgG
- Top Product
- Discover our top product TRIP4 Primary Antibody
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- Application Notes
- WB 1:500-1:1000, IHC 1:50-1:100
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 2 mg/mL
- Buffer
- PBS with 0.05 % Proclin300 and 50 % glycerol, pH 7.4.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- TRIP4 (Thyroid Hormone Receptor Interactor 4 (TRIP4))
- Alternative Name
- TRIP4 (TRIP4 Products)
- Synonyms
- TRIP4 antibody, ASC-1 antibody, ASC1 antibody, HsT17391 antibody, im:7143009 antibody, si:busm1-221i3.1 antibody, si:dkey-173l11.4 antibody, zgc:153348 antibody, 4930558E03Rik antibody, Asc1 antibody, BB191711 antibody, thyroid hormone receptor interactor 4 antibody, thyroid hormone receptor interactor 4 L homeolog antibody, TRIP4 antibody, TREPR_2022 antibody, trip4 antibody, trip4.L antibody, Trip4 antibody
- Background
- This gene encodes a subunit of the tetrameric nuclear activating signal cointegrator 1 (ASC-1) complex, which associates with transcriptional coactivators, nuclear receptors and basal transcription factors to facilitate nuclear receptors-mediated transcription. This protein is localized in the nucleus and contains an E1A-type zinc finger domain, which mediates interaction with transcriptional coactivators and ligand-bound nuclear receptors, such as thyroid hormone receptor and retinoid X receptor alpha, but not glucocorticoid receptor. Mutations in this gene are associated with spinal muscular atrophy with congenital bone fractures-1 (SMABF1).
- Molecular Weight
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Observed_MW: 66 kDa
Calculated_MW: 66 kDa
- UniProt
- Q15650
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