CNNM4 anticorps (AA 565-593)
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- Antigène Voir toutes CNNM4 Anticorps
- CNNM4 (Cyclin M4 (CNNM4))
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Épitope
- AA 565-593
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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 CNNM4 est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Purification
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogène
- This CNNM4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 565-593 amino acids from the Central region of human CNNM4.
- Isotype
- Ig Fraction
- Top Product
- Discover our top product CNNM4 Anticorps primaire
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- Indications d'application
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For WB starting dilution is: 1:1000
For IHC-P starting dilution is: 1:50~100 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.5 mg/mL
- Buffer
- Supplied in PBS with 0.09 % (W/V) sodium azide.
- 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
- 4 °C,-20 °C
- Stockage commentaire
- Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
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- Antigène
- CNNM4 (Cyclin M4 (CNNM4))
- Autre désignation
- CNNM4 (CNNM4 Produits)
- Synonymes
- anticorps DKFZp468E0110, anticorps ACDP4, anticorps 5430430O18Rik, anticorps Acdp4, anticorps cyclin and CBS domain divalent metal cation transport mediator 4, anticorps cyclin M4, anticorps CNNM4, anticorps CpipJ_CPIJ006743, anticorps cnnm4, anticorps Cnnm4
- Sujet
- This gene encodes a member of the ancient conserved domain containing protein family. Members of this protein family contain a cyclin box motif and have structural similarity to the cyclins. The encoded protein may play a role in metal ion transport. Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy and amelogenesis imperfecta. [provided by RefSeq].
- Poids moléculaire
- 87 kDa
- ID gène
- 26504
- UniProt
- Q6P4Q7
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