Protein SSUH2 homolog Antibodies

AND SSUH2 ELISA kits, Protein SSUH2 homolog Proteins

Many biological assays use antibodies to detect Protein SSUH2 homolog, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Protein SSUH2 homolog in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Protein SSUH2 homolog antibodies...

We validate the specificity of these antibodies to Protein SSUH2 homolog by testing them on tissues known to express SSUH2 positively and negatively. Browse below to find the SSUH2 antibody that suites your experiment. We have 1 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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SSUH2 Infographic by Boster Bio

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C3orf32 (SSUH2) (NM_015931) Human Over-expression Lysate

Human

$628
Cat # LS051066
20 µg, 100 µg

SSUH2 Overview

Facts about Protein SSUH2 homolog.

SSUH2 3D structure. Source: alphafold

Protein SSUH2 homolog (SSUH2)

Plays a role in odontogenesis. .

Gene Information

Human
Gene Name:	SSUH2
Uniprot:	Q9Y2M2
Entrez:	51066

Family

Belongs to:

No superfamily

Alternative Names

C3orf32 chromosome 3 open reading frame 32; fls485; SSU-2

Molecular Weight

Mass (kDA):
39.845 kDA

Genomic Context


Human

Location:	3p25.3
Sequence:	3; NC_000003.12 (8619400..8745035, complement)

Tissue Specificity

Expressed in enterocytes of small and large intestinal mucosa (at protein level). Expressed in chromaffine and interstitial cells. Expressed in peripheral blood and gingival cells (PubMed:27680507).

Subcellular Localizations

Cytoplasm. Nucleus.

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SSUH2

References

PMID: 20205943 by Reinartz A., et al. Small intestinal mucosa expression of putative chaperone fls485.

PMID: 27680507 by Xiong F., et al. Mutation in SSUH2 causes autosomal-dominant dentin dysplasia type I.