USB1 Antibodies

AND USB1 ELISA kits, USB1 Proteins

Many biological assays use antibodies to detect USB1, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with USB1 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop USB1 antibodies...

We validate the specificity of these antibodies to USB1 by testing them on tissues known to express USB1 positively and negatively. Browse below to find the USB1 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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USB1 Infographic by Boster Bio

All USB1 Products

Product

Figures

Specificity

Applications

Price

C16orf57 (USB1) (NM_024598) Human Recombinant Protein

$1249
Cat # PROTQ9BQ65
20 µg

Anti-C16orf57 (USB1) Mouse Monoclonal Antibody [Clone ID: OTI1B1]

Human

$523
Cat # M07652
100 µl

USB1 Overview

Facts about U6 snRNA phosphodiesterase.

USB1 3D structure. Source: alphafold

U6 snRNA phosphodiesterase (USB1)

Phosphodiesterase responsible for the U6 snRNA 3' end processing. Acts as an exoribonuclease (RNase) responsible for trimming the poly(U) tract of the past nucleotides from the pre-U6 snRNA molecule, leading to the formation of adult U6 snRNA 3' end-terminated using a 2',3'-cyclic phosphate.

Gene Information

Human
Gene Name:	USB1
Uniprot:	Q9BQ65
Entrez:	79650

Family

Belongs to:

2H phosphoesterase superfamily

Alternative Names

C16orf57; chromosome 16 open reading frame 57; FLJ13154; HVSL motif containing 1; HVSL1; hypothetical protein LOC79650; PN

Molecular Weight

Mass (kDA):
30.268 kDA

Genomic Context


Human

Location:	16q21
Sequence:	16; NC_000016.10 (57999603..58021618)

Subcellular Localizations

Nucleus.

Diseases

Rothmund-thomson Syndrome
Dyskeratosis Congenita
Dyskeratosis

Pathways

Telomere Maintenance
Dna Repair
Cell Growth
Oxidative Phosphorylation
Localization

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/USB1

References

PMID: 20004881 by Volpi L., et al. Targeted next-generation sequencing appoints c16orf57 as clericuzio- type poikiloderma with neutropenia gene.

PMID: 20503306 by Tanaka A., et al. Identification of a homozygous deletion mutation in C16orf57 in a family with Clericuzio-type poikiloderma with neutropenia.