The C15orf41 Polyclonal Antibody (PAC042818) is a highly specific antibody designed for researchers studying the C15orf41 protein, also known as FLJ40409. This antibody, raised in rabbits, is highly reactive with human samples and has been validated for use in various applications including Western blot and immunohistochemistry.C15orf41 is a protein that plays a role in various cellular processes and has been implicated in certain diseases. The antibody binds specifically to the C15orf41 protein, allowing for its detection and analysis in different cell types and tissues.
This makes it ideal for studies in cell biology, molecular biology, and disease research.Research involving C15orf41 is still ongoing, and the antibody provides a valuable tool for scientists looking to uncover the functions and mechanisms of this protein. By understanding the role of C15orf41 in cellular pathways and disease development, researchers may be able to develop targeted therapies for conditions associated with its dysregulation.
Antibody Name:
C15orf41 Antibody (PACO42818)
Antibody SKU:
PACO42818
Size:
50ug
Host Species:
Rabbit
Tested Applications:
ELISA, WB
Recommended Dilutions:
ELISA:1:2000-1:10000, WB:1:500-1:2000
Species Reactivity:
Human
Immunogen:
Recombinant Human Uncharacterized protein C15orf41 protein (1-183AA)
Western blot. All lanes: C15orf41 antibody at 1.5µg/ml. Lane 1: K562 whole cell lysate. Lane 2: HepG2 whole cell lysate. Lane 3: U251 whole cell lysate. Secondary. Goat polyclonal to rabbit IgG at 1/10000 dilution. Predicted band size: 33, 22 kDa. Observed band size: 33 kDa.
Synonyms:
Uncharacterized protein C15orf41 (Protein HH114), C15orf41
UniProt Protein Function:
C15orf41: 2 isoforms of the human protein are produced by alternative splicing.Chromosomal Location of Human Ortholog: 15q14Disease: Anemia, Congenital Dyserythropoietic, Type Ib
UniProt Protein Details:
NCBI Summary:
This gene encodes a protein with two predicted helix-turn-helix domains. Mutations in this gene were found in families with congenital dyserythropoietic anemia type Ib. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]
