Recombinant NR1D1 Monoclonal Antibody (E-AB-81587)

For research use only.
Verified Samples |
Verified Samples in WB: K562, C6, 3T3, Hela Verified Samples in IF: Hela cells |
Dilution | WB 1:500-1:1000, IF 1:20-1:100 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human, Mouse, Rat |
Applications | WB, IF |
Clonality | Rabbit Monoclonal |
Immunogen | A synthetic peptide of human NR1D1 |
Abbre | NR1D1 |
Synonyms | EAR-1, EAR1, ERBA-related 1, NR1D1, Nr1d1, Nuclear receptor Rev ErbA alpha, Nuclear receptor subfamily 1 group D member 1, Rev erbAalpha, Rev erbalpha, Rev-ErbAalpha, Rev-erbA-alpha, Reverba, THRA1, THRAL, Thyroid hormone recept, Thyroid hormone receptor, alpha like, hRev |
Swissprot | |
Calculated MW | 67 kDa |
Observed MW |
67 kDa
Western blotting is a method for detecting a certain protein in a complex sample based on the specific binding of antigen and antibody. Different proteins can be divided into bands based on different mobility rates. The mobility is affected by many factors, which may cause the observed band size to be inconsistent with the expected size. The common factors include: 1. Post-translational modifications: For example, modifications such as glycosylation, phosphorylation, methylation, and acetylation will increase the molecular weight of the protein. 2. Splicing variants: Different expression patterns of various mRNA splicing bodies may produce proteins of different sizes. 3. Post-translational cleavage: Many proteins are first synthesized into precursor proteins and then cleaved to form active forms, such as COL1A1. 4. Relative charge: the composition of amino acids (the proportion of charged amino acids and uncharged amino acids). 5. Formation of multimers: For example, in protein dimer, strong interactions between proteins can cause the bands to be larger. However, the use of reducing conditions can usually avoid the formation of multimers. If a protein in a sample has different modified forms at the same time, multiple bands may be detected on the membrane. |
Cellular Localization | Nucleus. |
Concentration | 300 μg/mL |
Buffer | 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.05% stabilizer and 0.05% protective protein. |
Purification Method | Affinity Purified |
Research Areas | Cancer, Epigenetics and Nuclear Signaling, Neuroscience, Signal Transduction |
Clone No. | R05-8B1 |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
background | This gene encodes a transcription factor that is a member of the nuclear receptor subfamily 1. The encoded protein is a ligand-sensitive transcription factor that negatively regulates the expression of core clock proteins. In particular this protein represses the circadian clock transcription factor aryl hydrocarbon receptor nuclear translocator-like protein 1 (ARNTL). This protein may also be involved in regulating genes that function in metabolic, inflammatory and cardiovascular processes. |
Other Clones
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Other Formats
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Unconjugated
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