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For research use only.

Verified Samples Verified Samples in WB: MCF-7, Mouse brain, Rat brain
Verified Samples in IHC: Mouse testis
Verified Samples in IF: Human appendix
Dilution WB 1:500-1:2000,  IHC 1:100-1:200,  IF 1:100-1:300
Isotype IgG
Host Mouse
Reactivity Human,  Mouse,  Rat
Applications WB,  IHC-p,  IF
Clonality Monoclonal
Immunogen Recombinant Protein
Abbre MICU1
Synonyms Allergen Hom s 4,  Atopy-related autoantigen CALC,  CALC,  Calcium uptake protein 1,  Calcium-binding atopy-relate,  ara CALC,  atopy related autoantigen,  atopy related autoantigen CALC,  calcium binding atopy related autoantigen 1,  calcium uptake protein 1,  mitochondrial
Swissprot
Observed MW 55 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 Mitochondrion inner membrane.
Tissue Specificity Expressed in epithelial cell line. Strongly expressed in epidermal keratinocytes and dermal endothelial cells.
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 Cancer,  Metabolism,  Immunology,  Signal Transduction
Clone No. 4E7
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 an essential regulator of mitochondrial Ca2+ uptake under basal conditions. The encoded protein interacts with the mitochondrial calcium uniporter, a mitochondrial inner membrane Ca2+ channel, and is essential in preventing mitochondrial Ca2+ overload, which can cause excessive production of reactive oxygen species and cell stress. Alternatively spliced transcript variants encoding different isoforms have been described. MICU1 (Mitochondrial Calcium Uptake 1) is a Protein Coding gene. Diseases associated with MICU1 include Myopathy With Extrapyramidal Signs and Fish Allergy. Among its related pathways are Ca, cAMP and Lipid Signaling. GO annotations related to this gene include calcium ion binding and protein heterodimerization activity. An important paralog of this gene is MICU3.
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Unconjugated

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