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YTHDF2 Antibody (P-13): sc-162426

 |  Datasheet

(Based on data analysis)
  • YTHDF2 Antibody (P-13) is a goat polyclonal IgG provided at 200 µg/ml
  • epitope mapping within an internal region of YTHDF2 of human origin
  • recommended for detection of YTHDF2 of mouse, rat and human origin by WB, IP, IF and ELISA; non cross-reactive with YTHDF1 or YTHDF3
  • blocking peptide, sc-162426 P
 

See additional YTHD Antibodies including YTHD, Ythdc1, YTHDC2, YTHDF1, YTHDF2 and YTHDF3.

Ordering InformationGene Info
Recommended Support Products:
(click button of application of choice)
WB   IP   IF   siRNA  
Set Currency

 Ordering Information
Product NameCatalog #UnitPriceQtyAdd 
YTHDF2 Antibody (P-13) sc-162426 200 µg/ml $279
YTHDF2 (P-13) P sc-162426 P
(peptide)
 100 µg/0.5 ml $61
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
YTHDF2 siRNA (h) sc-78661 10 µM $258
YTHDF2 siRNA (m) sc-155424 10 µM $258
YTHDF2 (h)-PR sc-78661-PR 10 µM, 20 µl $23
YTHDF2 (m)-PR sc-155424-PR 10 µM, 20 µl $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
YTHDF2 shRNA Plasmid (h) sc-78661-SH 20 µg $520
YTHDF2 shRNA Plasmid (m) sc-155424-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
YTHDF2 shRNA (h) Lentiviral Particles sc-78661-V 200 µl $625
YTHDF2 shRNA (m) Lentiviral Particles sc-155424-V 200 µl $625
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human YTHDF2 51441 1p35.3 Q9Y5A9
 610640
Mouse Ythdf2 213541 4 D2.3 NP_663368
 N/A
 

The YTH domain family protein family (YTHDF) includes YTHDF1, YTHDF2 and TYHDF3. YTHDF2 (YTH domain family, member 2), also designated high-glucose-regulated protein 8, CLL-associated antigen KW-14 or renal carcinoma antigen NY-REN-2, is a 579 amino acid protein that also contains one YTH domain and exists as two alternatively spliced isoforms. Expressed in pancreas, testis and placenta, YTHDF2 has been identified as a translocation partner gene for RUNX1 and is encoded by a gene mapping to human chromosome 1p35.3. Human chromosome 1 spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome.