Protein C10 Antibodies

AND C12orf57 ELISA kits, Protein C10 Proteins

Many biological assays use antibodies to detect Protein C10, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Protein C10 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Protein C10 antibodies...

We validate the specificity of these antibodies to Protein C10 by testing them on tissues known to express C12orf57 positively and negatively. Browse below to find the C12orf57 antibody that suites your experiment. We have 2 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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C12orf57 Infographic by Boster Bio

All C12orf57 Products

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Price

GRCC10 (C12orf57) (NM_138425) Human Recombinant Protein

$1062
Cat # PROTQ99622
20 µg

GRCC10 (C12orf57) (NM_138425) Human Over-expression Lysate

Human

$628
Cat # LS113246
100 µg

C12orf57 Overview

Facts about Protein C10.

C12orf57 3D structure. Source: alphafold

Protein C10 (C12orf57)

In brain, might be required for corpus callusum development. .

Gene Information

Human
Gene Name:	C12orf57
Uniprot:	Q99622
Entrez:	113246

Family

Belongs to:

UPF0456 family

Alternative Names

C10; C10GRCC10; chromosome 12 open reading frame 57; GRCC10; likely ortholog of mouse gene rich cluster, C10; protein C10

Molecular Weight

Mass (kDA):
13.178 kDA

Genomic Context


Human

Location:	12p13.31
Sequence:	12; NC_000012.12 (6943438..6946003)

Tissue Specificity

Ubiquitously expressed, with higher expression in lung and fetal brain.

Subcellular Localizations

Cytoplasm.

Diseases

Temtamy syndrome (TEMTYS)

PTMs

Acetylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/C12orf57

References

PMID: 9074930 by Ansari-Lari M.A., et al. Large-scale sequencing in human chromosome 12p13: experimental and computational gene structure determination.

PMID: 23453666 by Akizu N., et al. Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.