UQCRB / Cytochrome b-c1 complex subunit 7 · Western blot design guide

Design a Western Blot for UQCRB

Source-linked UQCRB Western blot protocol options, expected-band and isoform facts, troubleshooting for weak or shifted signal, and recommended anti-UQCRB 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 UQCRB: expected band ~13.5 kDa, hero antibody A07958, catalog values and labelled standard workflow; separate PMC comparisons on the guide
Printable UQCRB Western blot protocol sheet — expected band ~13.5 kDa, antibody A07958, controls and PMC citations. Open the full UQCRB WB guide →

UQCRB Western Blot Experimental Design Guide

Expected bands, source-linked protocol options, controls and antibodies — the at-a-glance facts below, then the full design guide.

Must know before running
Expected band ~13.5 kDa
Gel 15% (standard starting point)
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 Acetylated
Caveat Modification-state controls
Gene-set association MSigDB Hallmark membership
Isoform 2 isoform(s)
Section 1

Source-Linked UQCRB Western Blot Protocol Options

The A07958 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 / lysateextracts of various cell lines, (catalog A07958)
Gel %15% (standard starting point)
Load20–30 µg total protein per lane; optimize for abundance (standard starting point)
TransferShort semi-dry transfer; verify retention (standard starting point)
Membrane0.2 µm PVDF (standard starting point)
BlockingBlocking buffer: 3% nonfat dry milk in TBST (catalog A07958)
Primary antibodyA07958 · 1:1000 (catalog A07958)
Primary incubationOvernight at 4 °C (standard starting point)
Secondary antibodyGoat Anti-Rabbit IgG, 1:10000 (catalog A07958)
Secondary incubation1 h at room temperature (standard starting point)
Wash3 × 5 min in TBST (standard starting point)
DetectionECL (catalog A07958)
Section 2

What Is the Expected UQCRB Western Blot Band Size?

UQCRB has a predicted mass of 13.5 kDa; its isoforms could affect migration, but no empirical band or distinct isoform pattern is established.

What am I looking at on my blot?
Single band near 13.5 kDaConsistent with the predicted UQCRB mass; confirm identity with controls
Two bands at different positionsCould reflect isoforms 1 and 2, but their migration is not established
Weak band in whole-cell lysateRecovery of this mitochondrial inner-membrane protein may be limited
Band away from 13.5 kDaIts identity and reason for altered migration require verification
💡Expected UQCRB appearanceUniProt predicts UQCRB at 13.5 kDa; no empirical band size or isoform migration is supplied, so verify any detected band with antibody and target-specific controls.
How each factor affects band size
UniProt predicted massPlaces the reference band near 13.5 kDa
Isoform 1Has no supplied isoform-specific mass or migration
Isoform 2Has no supplied isoform-specific mass or migration
Alternative splicing of isoforms 1 and 2Could alter apparent size, but distinct bands are not established
Why is my band missing or off?
SituationLikely causeNext action
No band in lysateRecovery of mitochondrial inner-membrane UQCRB may be limitedCheck mitochondrial enrichment and lysate preparation
Band higher than expectedThe supplied features do not establish the shiftCheck molecular-weight markers and confirm identity with target-specific controls
Band lower than expectedThe supplied features do not establish the shiftConfirm identity with a second antibody or target-depleted sample
Multiple bandsIsoforms 1 and 2 are listed, but their band positions are unknownUse isoform-specific or target-depletion controls to identify the bands
Weak or no signalMitochondrial inner-membrane protein recovery may be lowAssess mitochondrial enrichment and antibody performance with a positive control

Sample controls for UQCRB Western blot

🧪HPA-IHC candidate guidance (verify in WB): For positive controls for UQCRB in Western blot, you can use adrenal gland tissue, which shows 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 tissue is listed as not detected, so use siRNA knockdown or a KO line for a negative control.

HPA tissue expression evidence for UQCRB

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 →
Breast glandular cells High Protein (IHC) HPA →
Bronchus respiratory epithelial cells High Protein (IHC) HPA →
Caudate glial cells High Protein (IHC) HPA →

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

TissueCell typeLevelEvidenceSource
Soft tissue fibroblasts Low Protein (IHC) HPA →
Adipose tissue adipocytes Medium Protein (IHC) HPA →
Bone marrow hematopoietic cells Medium Protein (IHC) HPA →
Ovary ovarian stroma cells Medium Protein (IHC) HPA →
Smooth muscle smooth muscle cells Medium Protein (IHC) HPA →
Section 3

Advanced UQCRB Western Blot Tips

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

Where should the UQCRB band appear?
Band shift · The predicted mass is 13.5 kDa. No observed band position is supplied, so use 13.5 kDa as a starting point rather than an expected apparent mass.
Could UQCRB isoforms produce different bands?
Isoforms · UniProt lists isoforms 1 and 2. Isoform 2 replaces residues 87–111 with a longer alternative sequence, which could change its apparent size. Whether both isoforms are expressed or resolved on a blot is not established here.
Which UQCRB modifications matter when interpreting bands?
PTM · In UniProt coordinates, residue 2 is N-acetylalanine; lysines 12, 19, 78, 83 and 96 have listed modifications. Acetylation and succinylation are alternate annotations at positions 12 and 78. These features alone do not establish a visible shift or explain a mass difference.
Does this guide establish induction of UQCRB?
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 UQCRB Western blot?
Transfer · UQCRB has a predicted mass of 13.5 kDa. Choose transfer conditions and a membrane that retain a small protein, then verify transfer near 13.5 kDa. The supplied features do not specify one transfer method.
How should blocking be optimized?
Blocking · Standard workflow guidance: follow the A07958 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 UQCRB bands be quantified?
Quantitation · UQCRB is a peripheral protein on the matrix side of the mitochondrial inner membrane and a component of complex III. Keep mitochondrial sample preparation and loading consistent across lanes. If multiple bands appear, quantify a consistently identified band; the supplied features do not establish which band represents each isoform.
How should unexpected UQCRB bands be interpreted?
Interpretation · Compare them with the 13.5 kDa prediction and consider the two listed isoforms, including isoform 2’s replacement of residues 87–111. The listed modifications do not, by themselves, identify a shifted band. No observed band position is supplied for comparison.
Boster reagents

UQCRB 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 extracts of various cell lines, using UQCRB 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: 10s.
Anti-UQCRB Antibody
Cat # A07958

A07958 is listed as reactive with human, mouse, and rat UQCRB. Its Western blot image uses extracts from various cell lines, 25 µg per lane, and a 1:1000 primary dilution. The caption does not identify the cell lines.

Which to pick: A07958 is the only listed option. It has a Western blot image, but the unnamed cell lines do not establish which of the listed species were tested in that image.

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