EFHD1 Monoclonal Antibody (E-AB-22043)

For research use only.
Verified Samples |
Verified Samples in WB: Mouse spleen, Rat spleen Verified Samples in IHC: Mouse testis, Verified Samples in IF: Hela |
Dilution | WB 1:500-1:3000, IHC 1:50-1:300, IF 1:100-1:200 |
Isotype | IgG |
Host | Mouse |
Reactivity | Human, Mouse, Rat |
Applications | WB, IHC-p, IF |
Clonality | Monoclonal |
Immunogen | Synthetic Peptide |
Abbre | EFHD1 |
Synonyms | 4931430I01Rik, AI452351, DKFZp781H0842, EF hand domain containing 1, EF hand domain family, EF-hand domain-containing protein 1, EF-hand domain-containing protein D1, EFHD1, FLJ13612, MGC103094, MST133, MSTP133, Mitocalcin, PP3051, RGD1559565, Swiprosin, member D1 |
Swissprot | |
Observed MW |
27 kDa
The actual band is not consistent with the expectation.
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 | Extracellular region or secreted, extracellular exosome, Mitochondrion, mitochondrial inner membrane. |
Concentration | 1 mg/mL |
Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer, 0.5% protein protectant and 50% glycerol. |
Purification Method | Protein A purification |
Research Areas | Cell Biology |
Clone No. | 5K1 |
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 member of the EF-hand super family of calcium binding proteins, which are involved in a variety of cellular processes including mitosis, synaptic transmission, and cytoskeletal rearrangement. The protein encoded by this gene is composed of an N-terminal disordered region, proline-rich elements, two EF-hands, and a C-terminal coiled-coil domain. This protein has been shown to associate with the mitochondrial inner membrane, and in HeLa cells, acts as a novel mitochondrial calcium ion sensor for mitochondrial flash activation. Alternative splicing results in multiple transcript variants.EFHD1 (EF-Hand Domain Family Member D1) is a Protein Coding gene. GO annotations related to this gene include calcium ion binding. An important paralog of this gene is EFHD2. |
Other Clones
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Other Formats
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Unconjugated
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