E-AB-18928
FUNDC2 Polyclonal Antibody
Size
£106.20
Was £118.00
- SKU:
- E-AB-18928
- Additional Names:
- Cervical cancer oncogene 3,Cervical cancer proto oncogene 3 protein,DC44,FLJ33773,FUN14 domain containing 2,FUN14 domain containing protein 2,FUNDC 2,HCBP 6,HCBP6,HCC 3,HCC3,Hepatitis C virus core binding protein 6,MGC131676,MGC2495,OTT,OTTHUMP00000015441
- Application:
- IHC
- Concentration:
- 0.72 mg/ml
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Avoid freeze/thaw cycles.
- Supplier:
- Elabscience
- Host:
- Rabbit
- Reactivities:
- Human
- Buffer:
- Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
- Immunogen:
- Fusion protein of human FUNDC2
- Uniprot:
- Q9BWH2
- Synonyms:
- cervical cancer oncogene 3;cervical cancer proto-oncogene 3 protein;DC44;FUN14 domain-containing protein 2;HCBP6;HCC-3;HCC3;hepatitis C virus core-binding protein 6;PD03104
- Extra Details:
- FUNDC2 (FUN14 domain-containing protein 2), also known as HCC-3 (cervical cancer proto-oncogene 3 protein), HCBP6 (hepatitis C virus core-binding protein 6) or DC44, is a 189 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC2 maps to human chromosome Xq28. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
- Shipping Conditions:
- Blue Ice