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Product Name Methyltransferase like 10 Chinese Name 甲基转移酶样蛋白10抗体 Alias C10orf138; Chromosome 10 open reading frame 138; EC 2.1.1.-; Em:AC068896.3; FLJ13019; LOC399818; Methyltransferase like 10; Methyltransferase-like protein 10; Mettl10; MTL10_HUMAN; OTTHUMP00000020696. Research Area Cell biology immunology Immunogen Species Rabbit Clonality Polyclonal React Species (predicted: Human, Mouse, Rat, Pig, Cow, Sheep, ) Applications IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.Theoretical molecular weight 32kDa Cellular localization cytoplasmic Form Liquid Concentration 1mg/ml immunogen KLH conjugated synthetic peptide derived from human Methyltransferase like 10: 21-120/311 Lsotype IgG Purification affinity purified by Protein A Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. PubMed PubMed Product Detail METTL10 is a 291 amino acid protein that belongs to the methyltransferase superfamily and is encoded by a gene that maps to human chromosome 10q26.13. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Similarity:
Belongs to the methyltransferase superfamily.
SWISS:
Q5JPI9
Gene ID:
399818
Database links:Entrez Gene: 399818 Human
Entrez Gene: 72096 Mouse
SwissProt: Q5JPI9 Human
SwissProt: Q9D853 Mouse
Unigene: 468488 Human
Unigene: 28631 Mouse
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