METTL7A anticorps
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- Antigène Voir toutes METTL7A Anticorps
- METTL7A (Methyltransferase Like 7A (METTL7A))
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Reactivité
- Humain, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp METTL7A est non-conjugé
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Application
- Immunohistochemistry (IHC), Western Blotting (WB)
- Attributs du produit
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogène
- Recombinant fusion protein of human METTL7A (NP_054752.3).
- Isotype
- IgG
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- Indications d'application
- WB 1:500-1:2000 IHC 1:50-1:200
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- 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
- METTL7A (Methyltransferase Like 7A (METTL7A))
- Autre désignation
- METTL7A (METTL7A Produits)
- Synonymes
- anticorps AAM-B, anticorps 2210414H16Rik, anticorps 3300001H21Rik, anticorps Aam-B, anticorps Mettl7a, anticorps UbiE1, anticorps RGD1308407, anticorps MGC82719, anticorps zgc:153889, anticorps MGC145311, anticorps DKFZp459L026, anticorps methyltransferase like 7A, anticorps methyltransferase like 7A1, anticorps methyltransferase like 7A L homeolog, anticorps METTL7A, anticorps Mettl7a1, anticorps Mettl7a, anticorps mettl7a.L, anticorps mettl7a
- Sujet
- METTL7A (methyltransferase like 7A), also known as AAM-B, is a 244 amino acid protein that is thought to function as a methyltransferase and is encoded by a gene which maps to chromosome 12. Encoding over 1,100 genes, chromosome 12 comprises nearly 4.5 % of the human genome and is associated with a number of skeletal deformaties, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Chromosome 12 is also home to both a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and a natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Additionally, Trisomy 12p (three copies of the p arm of chromosome 12) leads to facial developmental defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism.
- Poids moléculaire
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Observed_MW: 28 kDa
Calculated_MW: 28 kDa
- ID gène
- 25840
- UniProt
- Q9H8H3
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