Protein C15orf41 Antibodies

AND C15orf41 ELISA kits, Protein C15orf41 Proteins

Many biological assays use antibodies to detect Protein C15orf41, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Protein C15orf41 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Protein C15orf41 antibodies...

We validate the specificity of these antibodies to Protein C15orf41 by testing them on tissues known to express C15orf41 positively and negatively. Browse below to find the C15orf41 antibody that suites your experiment. We have 0 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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C15orf41 Infographic by Boster Bio

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C15orf41 Overview

Facts about Protein C15orf41.

C15orf41 3D structure. Source: alphafold

Protein C15orf41 (C15orf41)

Gene Information

Human
Gene Name:	C15orf41
Uniprot:	Q9Y2V0
Entrez:	84529

Family

Belongs to:

No superfamily

Alternative Names

Chromosome 15 Open Reading Frame 41; HH114; Protein HH114; Uncharacterized Protein C15orf41

Molecular Weight

Mass (kDA):
32.264 kDA

Genomic Context


Human

Location:	15q14
Sequence:	15; NC_000015.10 (36579611..36810248)

Subcellular Localizations

Nucleus. Cytoplasm. Mainly nuclear.

Diseases

Anemia, congenital dyserythropoietic, 1B (CDAN1B)

PTMs

Phosphoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/C15orf41

References

PMID: 23716552 by Babbs C., et al. Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I.

PMID: 29885034 by Palmblad J., et al. Congenital dyserythropoietic anemia type 1: a case with novel compound heterozygous mutations in the C15orf41 gene.