Recombinant MLLT6 Monoclonal Antibody (AN301216L)
For research use only.
| Verified Samples | Verified Samples in WB: NIH/3T3 |
| Dilution | WB 1:1000-1:5000, |
| Isotype | IgG,κ |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Applications | WB |
| Clonality | Monoclonal;Recombinant |
| Immunogen | Recombinant Human MLLT6 protein |
| Abbre | MLLT6 |
| Synonyms | MLLT, AF17, MLLT6, Drosophila) translocated to 6, AF 17, ALL1-fused gene from chromosome 17 protein, FLJ23480, MLLT 6, Myeloid/lymphoid or mixed lineage leukemia (trithorax (Drosophila) homolog) translocated to 6, Myeloid/lymphoid or mixed lineage leukemia (trithorax homolog, Myeloid/lymphoid or mixed lineage leukemia translocated to 6, OTTHUMP00000164158, Protein AF 17, Protein AF-17, Trithorax homolog |
| Swissprot | |
| Calculated MW | 120 kDa |
| Observed MW |
120 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 {ECO:0000305}. |
| Concentration | 0.2 mg/mL |
| Buffer | PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant. |
| Purification Method | Protein A |
| Research Areas | Epigenetics and Nuclear Signaling |
| Clone No. | 4B3 |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | Ice bag |
| background | Enables histone binding activity and nucleosome binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within several processes, including renal potassium excretion; renal sodium excretion; and renal water absorption. Predicted to be active in nucleus. |
Other Clones
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Other Formats
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Unconjugated
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