UQCC1 Antibodies

AND UQCC1 ELISA kits, UQCC1 Proteins

Many biological assays use antibodies to detect UQCC1, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with UQCC1 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop UQCC1 antibodies...

We validate the specificity of these antibodies to UQCC1 by testing them on tissues known to express UQCC1 positively and negatively. Browse below to find the UQCC1 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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UQCC1 Infographic by Boster Bio

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UQCC (UQCC1) (NM_018244) Human Over-expression Lysate

UQCC (UQCC1) Human Over-expression Lysates NM_001184977

Human

$628
Cat # LS055245
20 µg, 100 µg

UQCC1 Overview

Facts about Ubiquinol-cytochrome-c reductase complex assembly factor 1.

UQCC1 3D structure. Source: alphafold

Ubiquinol-cytochrome-c reductase complex assembly factor 1 (UQCC1)

Required for the assembly of the ubiquinol-cytochrome c reductase complex (mitochondrial respiratory chain complex III or cytochrome b-c1 complicated ). Involved in cytochrome b translation and/or equilibrium.

Gene Information

Human
Gene Name:	UQCC1
Uniprot:	Q9NVA1
Entrez:	55245

Family

Belongs to:

CBP3 family

Alternative Names

Ubiquinol-cytochrome-c reductase complex assembly factor 1

Molecular Weight

Mass (kDA):
34.6 kDA

Genomic Context


Human

Location:	20q11.22
Sequence:	20; NC_000020.11 (35302566..35412142, complement)

Subcellular Localizations

Mitochondrion inner membrane. Cytoplasmic vesicle. Cytoplasmic vesicular structures.

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/UQCC1

References

PMID: 24385928 by Tucker E.J., et al. Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression.