METTL7A Polyclonal Antibody
€0.00
In stock
SKU
E-AB-62404
Catalog Number: E-AB-62404
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: WB,IHC
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: WB,IHC
Datasheet, Questions? Contact us!
Background:
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.
Research Area: Epigenetics and Nuclear Signaling
Synonyms:
METTL7A, AAM-B
Immunogen: Recombinant fusion protein of human METTL7A (NP_054752.3).
Swissprot: Q9H8H3
Gene ID: 25840
Calculated MW: 28 kDa
Observed MW: 28 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: "WB 1:500-1:2000 IHC 1:50-1:200"
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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.
Research Area: Epigenetics and Nuclear Signaling
Synonyms:
METTL7A, AAM-B
Immunogen: Recombinant fusion protein of human METTL7A (NP_054752.3).
Swissprot: Q9H8H3
Gene ID: 25840
Calculated MW: 28 kDa
Observed MW: 28 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: "WB 1:500-1:2000 IHC 1:50-1:200"
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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