UQCRC1 / Cytochrome b-c1 complex subunit 1, mitochondrial · Western blot design guide

Design a Western Blot for UQCRC1

Real validated UQCRC1 Western blot protocols, expected-band and isoform facts, troubleshooting for weak or shifted signal, and recommended anti-UQCRC1 WB antibodies. Everything you need to plan the experiment before you commit precious samples.

Evidence assembled September 2026 · For research use; verify linked source records and product datasheet before use
Western blot protocol sheet for UQCRC1: expected band ~52.6 kDa, hero antibody A06974-1, catalog values and labelled standard workflow; separate PMC comparisons on the guide
Printable UQCRC1 Western blot protocol sheet — expected band ~52.6 kDa, antibody A06974-1, controls and PMC citations. Open the full UQCRC1 WB guide →

UQCRC1 Western Blot Experimental Design Guide

Expected bands, validated protocols, controls and antibodies — the at-a-glance facts below, then the full design guide.

Must know before running
Expected band ~52.6 kDa
Observed band ~45 kDa
Gel 12% (catalog A06974-1)
Positive control ⓘ Adrenal gland (IHC candidate; verify WB) +4 more
Negative control ⓘ Suggested KO / knockdown lysate
Important caveats
Reasons your observed band may differ from the expected size.
PTM Phosphorylated + Acetylated
Caveat Band identity controls
Gene-set association MSigDB Hallmark membership
Isoform 1 isoform(s)
Section 1

Real Curated UQCRC1 Western Blot Protocols

The A06974-1 protocol combines labelled catalog values with standard starting conditions. Published comparisons retain their own sample, reagent and detection scope.

Recommended Western blot protocol parameters
Sample / lysatehuman Hela, human HepG2, human A549 (catalog A06974-1)
Gel %12% (catalog A06974-1)
Load30 ug; reducing conditions (catalog A06974-1)
Transfera nitrocellulose membrane at 150 mA for 50-90 minutes (catalog A06974-1)
Membranenitrocellulose membrane (catalog A06974-1)
Blocking5% non-fat milk/TBS for 1.5 hour at RT (catalog A06974-1)
Primary antibodyA06974-1 · 1:1000 (catalog A06974-1)
Primary incubationovernight at 4°C (catalog A06974-1)
Secondary antibodygoat anti-rabbit IgG-HRP, 1:5000 (catalog A06974-1)
Secondary incubation1.5 hour at RT (catalog A06974-1)
WashTBS-0.1%Tween 3 times with 5 minutes each (catalog A06974-1)
DetectionECL (catalog A06974-1)
Section 2

What Is the Expected UQCRC1 Western Blot Band Size?

UQCRC1 is predicted at 52.6 kDa, but antibody QC shows approximately 45 kDa; the cause of this difference is not established.

What am I looking at on my blot?
Band near 45 kDaEmpirical UQCRC1 band reported in reducing whole-cell lysates; confirm identity with controls
Band near 52.6 kDaNear the predicted sequence mass; identity requires confirmation
Faint band near 45 kDa in whole-cell lysateUQCRC1 signal may be limited by recovery of its mitochondrial membrane compartment
No band in a mitochondrial-depleted fractionConsistent with UQCRC1 localization at the mitochondrial inner membrane
💡Expected UQCRC1 appearanceUQCRC1 has a predicted mass of 52.6 kDa, while antibody QC reports a band near 45 kDa in reducing whole-cell lysates; the difference is unexplained, so confirm identity with ordinary controls.
How each factor affects band size
Predicted sequence mass52.6 kDa provides a reference, while observed migration is near 45 kDa
N6-acetyllysine at residues 111, 138, 163, and 248No visible band-size effect is established
N6-succinyllysine at residue 163An alternate modification at this site; no visible size effect is established
Phosphoserine at residue 212No visible band-size effect is established
Why is my band missing or off?
SituationLikely causeNext action
No band in lysateLimited recovery of mitochondrial inner-membrane materialCheck mitochondrial protein recovery and probe a mitochondrial loading control
Band lower than expectedThe reported 45 kDa band is below the 52.6 kDa predicted mass; the cause is unknownCompare with the reported QC pattern and confirm identity by knockdown or a second antibody
Band higher than expectedIdentity or migration of the extra band is uncertainCompare with the 45 kDa QC band and verify specificity by knockdown
Multiple bandsAdditional band identities are unestablished for the single listed isoformCompare controls and test which bands decrease after UQCRC1 knockdown
Weak or no signalLow mitochondrial protein recovery or low target abundance in the sampleCheck sample loading and mitochondrial enrichment
Fragments below expected sizePossible sample degradation; no fragment size is establishedPrepare fresh lysate with protease inhibitors and verify bands with a second antibody

Sample controls for UQCRC1 Western blot

🧪HPA-IHC candidate guidance (verify in WB): For positive controls for UQCRC1 in Western blot, you can use adrenal gland tissue, which has high HPA expression.
Positive control: Adrenal gland (IHC candidate; verify WB)
Negative control: Suggested KO / knockdown lysate
Loading controls: Run GAPDH, β-actin, and a total-protein stain alongside the samples.
⚠️Feasibility: No HPA tissue is listed as not detected, so use siRNA knockdown or a KO line for a negative control.

HPA tissue expression evidence for UQCRC1

Comprehensive Human Protein Atlas IHC scoring per tissue. Rows are taken directly from the HPA tissue chart — click any row's HPA link to view the source.

Higher expression tissues · candidate positive controls from IHC

TissueCell typeLevelEvidenceSource
Adrenal gland glandular cells High Protein (IHC) HPA →
Appendix glandular cells High Protein (IHC) HPA →
Bronchus respiratory epithelial cells High Protein (IHC) HPA →
Caudate glial cells High Protein (IHC) HPA →
Cerebellum cells in molecular layer High Protein (IHC) HPA →

Lower expression tissues · IHC evidence, not confirmed WB-negative controls

TissueCell typeLevelEvidenceSource
Adipose tissue adipocytes Low Protein (IHC) HPA →
Ovary ovarian stroma cells Low Protein (IHC) HPA →
Bone marrow hematopoietic cells Medium Protein (IHC) HPA →
Breast glandular cells Medium Protein (IHC) HPA →
Fallopian tube glandular cells Medium Protein (IHC) HPA →
Section 3

Advanced UQCRC1 Western Blot Tips

Deeper troubleshooting and optimisation questions for UQCRC1, answered from its protein features.

How should UQCRC1 band migration be interpreted?
Band shift · Use the separately labelled calculated mass and catalog-observed evidence above. A sequence annotation does not establish an observed migration shift. Verify target identity with orthogonal controls.
Could UQCRC1 isoforms explain multiple bands?
Isoforms · Only one isoform is supplied, with no alternative sequence. These features provide no isoform-based explanation for multiple bands; verify the identity of each band.
Which UQCRC1 modifications are listed?
PTM · In UniProt sequence numbering, N6-acetyllysine is listed at 111, 138, 163 and 248; N6-succinyllysine is an alternate modification at 163; and phosphoserine is listed at 212. These annotations alone do not establish a visible band shift.

Phosphoserine is listed at UniProt position 212. Its presence does not establish that phosphorylation causes a visible shift. Compare band patterns after phosphatase treatment if testing that possibility; keep UniProt numbering distinct from any antibody or paper numbering.
Does this guide establish induction of UQCRC1?
Induction · No general induction response is established by this guide. A pathway or gene-set association is not evidence of induction in a particular specimen. Verify the relevant treatment and control in a target-specific experiment.
What transfer method to use for UQCRC1 Western blot?
Transfer · Choose transfer conditions suitable for a roughly 45–53 kDa protein and check transfer with a total-protein stain. UQCRC1 is a peripheral protein on the matrix side of the mitochondrial inner membrane; these features do not specify wet or semi-dry transfer.
How should blocking be optimized?
Blocking · Standard workflow guidance: follow the A06974-1 datasheet where specified. Otherwise compare 5% milk or 5% BSA in TBST; for a phospho-specific assay start with BSA. Optimize background and specific signal with matched controls.
How should I quantify UQCRC1 across samples?
Quantitation · Measure the same verified UQCRC1 band at exposures within the linear detection range and normalize to total protein. Because UQCRC1 is mitochondrial, changes in mitochondrial content can affect comparisons between whole-cell samples.
Why might UQCRC1 run near 45 kDa instead of 52.6 kDa?
Interpretation · The observed band is about 45 kDa, while the predicted mass is 52.6 kDa. A transit peptide is listed as a keyword, but no cleavage position is supplied, so these features do not establish why the masses differ. Confirm the band’s identity experimentally.

Compare them with the observed approximately 45 kDa band and the 52.6 kDa predicted mass, then test antibody specificity using UQCRC1 depletion. The supplied record lists one isoform and several modifications, but neither establishes the identity of an additional band.
Boster reagents

UQCRC1 Western Blot Antibodies

Catalog antibodies with Western blot application and product-specific WB images. Evaluate suitability with the reported sample, controls and experimental conditions.

Real WB data Western blot analysis of UQCRC1 using anti-UQCRC1 antibody (A06974-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: monkey COS-7 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UQCRC1 antigen affinity purified polyclonal antibody (A06974-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for UQCRC1 at approximately 45 kDa. The expected band size for UQCRC1 is at 53 kDa.
Anti-UQCRC1 Antibody
Cat # A06974-1
Real WB data Western blot analysis of extracts of various cell lines, using UQCRC1 antibody at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit . Exposure time: 1s.
Anti-UQCRC1 Antibody
Cat # A06974

Both listed anti-UQCRC1 antibodies have Western blot images. A06974-1 shows human cell, monkey cell, and rat and mouse tissue lysates; its reported band is approximately 45 kDa versus an expected 53 kDa. A06974’s caption reports various cell line extracts without naming them.

Which to pick: For monkey samples, A06974-1 is the only listed option with monkey reactivity and a named monkey sample in its WB caption. For human, mouse, or rat samples, both list reactivity; A06974-1 provides more specific sample details, though its observed band differs from the expected size.

Source: BosterBio UQCRC1 gene-info card — filtered to Western-blot-capable antibodies; each card shows that product's actual WB validation figure.