Family with Sequence Similarity 36, Member A (FAM36A) (C-Term) Peptide
FAM36A
Reactivité: Humain
Hôte: Synthetic
BP, WB
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- Antigène Tous les produits FAM36A
- FAM36A (Family with Sequence Similarity 36, Member A (FAM36A))
- Protein Region
- C-Term
- Origine
- Humain
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Séquence
- VTLGCWFHCR YNYAKQRIQE RIAREEIKKK ILYEGTHLDP ERKHNGSSSN
- Attributs du produit
- This is a synthetic peptide designed for use in combination with anti- FAM36A Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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- Indications d'application
- Optimal working dilution should be determined by the investigator.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Stock
- -20 °C
- Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Antigène
- FAM36A (Family with Sequence Similarity 36, Member A (FAM36A))
- Synonymes
- FAM36A Peptide, 2310005N03Rik Peptide, Fam36a Peptide, RGD1309105 Peptide, cox20 Peptide, fam36a Peptide, COX20, cytochrome c oxidase assembly factor Peptide, COX20 Cox2 chaperone Peptide, COX20 cytochrome C oxidase assembly factor Peptide, COX20 cytochrome c oxidase assembly factor L homeolog Peptide, COX20 Peptide, Cox20 Peptide, cox20.L Peptide
- Sujet
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This gene encodes a protein that plays a role in the assembly of cytochrome C oxidase, an important component of the respiratory pathway. It contains two transmembrane helices and localizes to the mitochondrial membrane. Mutations in this gene can cause mitochondrial complex IV deficiency, which results in ataxia and muscle hypotonia. There are multiple pseudogenes for this gene. Alternative splicing results in multiple transcript variants.
Alias Symbols: FAM36A
Protein Size: 130 - ID gène
- 116228
- NCBI Accession
- NM_001312871, NP_001299800
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