CYB5A anticorps (AA 1-100)
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- Antigène Voir toutes CYB5A Anticorps
- CYB5A (Cytochrome B5 Type A (Microsomal) (CYB5A))
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Épitope
- AA 1-100
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp CYB5A est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
- Séquence
- MAEQSDEAVK YYTLEEIQKH NHSKSTWLIL HHKVYDLTKF LEEHPGGEEV LREQAGGDAT ENFEDVGHST DAREMSKTFI IGELHPDDRP KLNKPPETLI
- Réactivité croisée
- Humain, Souris, Rat
- Attributs du produit
- Polyclonal Antibodies
- Purification
- Affinity purification
- Immunogène
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-100 of human CYB5A (NP_683725.1).
- Isotype
- IgG
- Top Product
- Discover our top product CYB5A Anticorps primaire
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- Indications d'application
- WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200
- Commentaires
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HIGH QUALITY
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- CYB5A (Cytochrome B5 Type A (Microsomal) (CYB5A))
- Autre désignation
- CYB5A (CYB5A Produits)
- Synonymes
- anticorps CYB5, anticorps MCB5, anticorps Cyb5, anticorps cyb5, anticorps zgc:64123, anticorps wu:fb44a11, anticorps MGC80327, anticorps 0610009N12Rik, anticorps Cyb5a, anticorps CYB5A, anticorps cytochrome b5 type A, anticorps cytochrome b5 type A (microsomal), anticorps cytochrome b5 type A (microsomal) L homeolog, anticorps cytochrome b5, anticorps CYB5A, anticorps Cyb5a, anticorps cyb5a, anticorps cyb5a.L, anticorps LOC100328915, anticorps LOC100735904
- Sujet
- The protein encoded by this gene is a membrane-bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin, which is required for stearyl-CoA-desaturase activity. Defects in this gene are a cause of type IV hereditary methemoglobinemia. Three transcript variants encoding different isoforms have been found for this gene.,CYB5A,CYB5,MCB5,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Cytochromes,Mitochondrial markers,CYB5A
- Poids moléculaire
- 11 kDa/14 kDa/15 kDa
- ID gène
- 1528
- UniProt
- P00167
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