Recombinant ALDH3A1 Monoclonal Antibody (AN300160P)

For research use only.
Verified Samples | Verified Samples in WB: A549 |
Dilution | WB 1:500-1:2000, |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human |
Applications | WB |
Clonality | Rabbit Monoclonal |
Immunogen | Recombinant Human ALDH3A1 Protein |
Abbre | ALDH3A1 |
Synonyms | ALDH, ALDH3A, ALDH3, ALDH3A1, Acetaldehyde dehydrogenase 3, AHD 4, AHD C, AHD4, AHDC, AL3A1, Aldehyde dehydrogenase, Aldehyde dehydrogenase 3, Aldehyde dehydrogenase 3 family member A1, Aldehyde dehydrogenase 3A1, Aldehyde dehydrogenase class 3, Aldehyde dehydrogenase dimeric NADP preferring, Aldehyde dehydrogenase family 3, Aldehyde dehydrogenase family 3 member A1, Aldehyde dehydrogenase family 3 subfamily A1, Aldehyde dehydrogenase isozyme 3, Aldehyde dehydrogenase type III, ALDH 3, ALDH 3A1, ALDH III, ALDH3 A1, ALDH3A 1, ALDH3A10, ALDHIII, dimeric NADP-preferring, member 1, MGC10406, Stomach aldehyde dehydrogenase, stomach type, subfamily A, Tumor associated aldehyde dehydrogenase tumor ALDH |
Swissprot | |
Calculated MW | 50 kDa |
Observed MW |
50 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. |
Concentration | 1 mg/mL |
Buffer | 0.2 μm filtered solution in PBS |
Purification Method | Protein A |
Research Areas | Signal Transduction, Neuroscience, Cell Biology, Metabolism |
Clone No. | 2D4 |
Conjugation | Unconjugated |
Storage | This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles. |
Shipping | Ice bag |
background | Aldehyde dehydrogenase 3A1 (ALDH3A1) is a metabolic enzyme that catalyzes the oxidation of various aldehydes. Certain types of epithelial tissues in mammals, especially those continually exposed to environmental stress (e.g., corneal epithelium), express ALDH3A1 at high levels and its abundance in such tissues is perceived to help to maintain cellular homeostasis under conditions of oxidative stress. Metabolic as well as non-metabolic roles for ALDH3A1 have been associated with its mediated resistance to cellular oxidative stress. Aldehyde dehydrogenase 1A1 (ALDH1A1) and ALDH3A1 are corneal crystallins. They protect inner ocular tissues from ultraviolet radiation (UVR)-induced oxidative damage through catalytic and non-catalytic mechanisms. |
Other Clones
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