MTERF1 / Transcription termination factor 1, mitochondrial · Western blot design guide

Design a Western Blot for MTERF1

Source-linked MTERF1 Western blot protocol options, expected-band and isoform facts, troubleshooting for weak or shifted signal, and recommended anti-MTERF1 WB antibodies. Everything you need to plan the experiment before you commit precious samples.

Evidence assembled October 2026 · For research use; verify linked source records and product datasheet before use
Western blot protocol sheet for MTERF1: expected band ~45.8 kDa, hero antibody A30769, catalog values and labelled standard workflow; separate PMC comparisons on the guide
Printable MTERF1 Western blot protocol sheet — expected band ~45.8 kDa, antibody A30769, controls and PMC citations. Open the full MTERF1 WB guide →

MTERF1 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 ~45.8 kDa
Observed band 72 kDa
Gel 12–15% (standard starting point)
Positive control ⓘ Adrenal gland (IHC candidate; verify WB) +4 more
Negative control ⓘ Adipose tissue (IHC candidate; verify WB)
Important caveats
Reasons your observed band may differ from the expected size.
PTM Phosphorylated
Caveat Peptide-blocking control
Gene-set association MSigDB C7 membership
Isoform 1 isoform(s)
Section 1

Source-Linked MTERF1 Western Blot Protocol Options

The A30769 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 / lysatethe lysates from HUVECcells (catalog A30769)
Gel %12–15% (standard starting point)
Load20–30 µg total protein per lane; optimize for abundance (standard starting point)
TransferStandard semi-dry transfer; verify efficiency (standard starting point)
Membrane0.45 µm PVDF (standard starting point)
Blocking5% milk or 5% BSA in TBST (standard starting point)
Primary antibodyA30769; use the WB datasheet starting dilution (standard starting point)
Primary incubationOvernight at 4 °C (standard starting point)
Secondary antibodySpecies-matched HRP conjugate at validated dilution (standard starting point)
Secondary incubation1 h at room temperature (standard starting point)
Wash3 × 5 min in TBST (standard starting point)
DetectionECL; bracket exposures to avoid saturation (standard starting point)
Section 2

What Is the Expected MTERF1 Western Blot Band Size?

MTERF1 is predicted at 45.8 kDa, while antibody QC reports a 72 kDa band; the cause of the difference is not established.

What am I looking at on my blot?
Band near 72 kDaMatches the empirical MTERF1 band; confirm its identity with antibody controls
Band near 45.8 kDaNear the predicted mass; confirm its identity
One dominant bandConsistent with the annotated monomer and single isoform
Weak band in whole-cell lysateMitochondrial localization may limit detection
💡Expected MTERF1 appearanceMTERF1 has a predicted mass of 45.8 kDa and an empirical band at 72 kDa; the cause of the difference is not established, so confirm band identity with antibody controls.
How each factor affects band size
UniProt predicted massProvides a sequence-based reference of 45.8 kDa
Predicted mass in daltons45,778 Da rounds to 45.8 kDa
Predicted mass versus observed migrationThe empirical band is at 72 kDa, with no established cause for the difference
Predicted mass as a band referenceA band near 45.8 kDa would require identity confirmation
Why is my band missing or off?
SituationLikely causeNext action
No band in lysateMitochondrial MTERF1 may be scarce in whole-cell lysateCheck a mitochondrial-enriched fraction and a positive-control lysate
Band higher than expectedThe reported 72 kDa band exceeds the 45.8 kDa prediction for an unknown reasonCheck peptide competition and confirm with an independent antibody
Band lower than expectedBand identity or sample integrity is uncertainCheck sample handling and confirm with an independent antibody
Multiple bandsOnly one isoform is annotated; additional band identities are uncertainCompare peptide-blocked and unblocked lanes
Weak or no signalMTERF1 abundance in the sampled lysate may be lowUse a positive-control lysate or mitochondrial enrichment

Sample controls for MTERF1 Western blot

🧪HPA-IHC candidate guidance (verify in WB): For positive controls for MTERF1 in Western blot, you can use adrenal gland lysate, which has medium HPA signal.
Positive control: Adrenal gland (IHC candidate; verify WB)
Negative control: Adipose tissue (IHC candidate; verify WB)
Loading controls: Run GAPDH, β-actin, and a total-protein stain alongside the samples.
⚠️Feasibility: MTERF1 is mitochondrial, so retain mitochondria when preparing the positive-control lysate.

HPA tissue expression evidence for MTERF1

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 Medium Protein (IHC) HPA →
Appendix glandular cells Medium Protein (IHC) HPA →
Bone marrow hematopoietic cells Medium Protein (IHC) HPA →
Bronchus respiratory epithelial cells Medium Protein (IHC) HPA →
Caudate neuronal cells Medium Protein (IHC) HPA →

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

TissueCell typeLevelEvidenceSource
Adipose tissue adipocytes Not detected Protein (IHC) HPA →
Lymph node germinal center cells Not detected Protein (IHC) HPA →
Oral mucosa squamous epithelial cells Not detected Protein (IHC) HPA →
Ovary ovarian stroma cells Not detected Protein (IHC) HPA →
Parathyroid gland glandular cells Not detected Protein (IHC) HPA →
Section 3

Advanced MTERF1 Western Blot Tips

Deeper troubleshooting and optimisation questions for MTERF1, answered from its protein features.

How should MTERF1 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 an alternative isoform explain another MTERF1 band?
Isoforms · The supplied record lists one isoform and no alternative sequence. Do not assign a second band to a documented MTERF1 isoform on this evidence alone.
Does phosphorylation explain the 72 kDa band?
PTM · MTERF1 has a phosphoprotein keyword, but no modified residue or site is listed. That annotation alone does not demonstrate a visible band shift or explain the difference between 45.8 and 72 kDa.
Does this guide establish induction of MTERF1?
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 MTERF1 Western blot?
Transfer · The features do not specify a transfer method. Check transfer at both the predicted 45.8 kDa position and the reported 72 kDa position before interpreting a missing or unexpected signal.
How should blocking be optimized?
Blocking · Standard workflow guidance: follow the A30769 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 MTERF1 bands be quantified?
Quantitation · Define the band used for quantitation consistently across samples. MTERF1 is annotated as mitochondrial and monomeric, but these features do not establish that a 72 kDa band represents the monomer. Confirm the band's identity before comparing its intensity.
Why is the observed MTERF1 band 72 kDa instead of 45.8 kDa?
Interpretation · The supplied predicted mass is 45.8 kDa, while the reported apparent band is 72 kDa. The listed features do not establish the cause of this difference. Verify band identity before assigning the 72 kDa signal to MTERF1.

MTERF1 is mitochondrial and has a transit-peptide keyword, but no cleavage position is supplied. Import processing may affect mass; these features cannot establish that it produces the 72 kDa band.

The record lists a monomer, one isoform, and no glycosylation sites or modified residue positions. These features do not identify additional bands. Check band identity before attributing them to processing or modification.
Boster reagents

MTERF1 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 the lysates from HUVECcells using MTERF antibody.
Anti-MTERF Antibody
Cat # A30769
Real WB data Western blot (WB) analysis of MTERF polyclonal antibody at 1:500 dilution Lane1:Hela cell lysate Lane2:Raw264.7 cell lysate Lane3:PC12 cell lyate
Anti-MTERF MTERF1 Antibody
Cat # A08459-1

The catalog reports two anti-MTERF1 antibodies, A30769 and A08459-1, with stated Human, Mouse, and Rat reactivity. Both have Western blot images. The captions document specific cell lysates; they do not establish performance across all samples of those species.

Which to pick: For HUVEC lysates, A30769 has a matching WB example. A08459-1 has WB examples using HeLa, Raw264.7, and PC12 lysates at 1:500. Choose by the sample and reported conditions; both list Human, Mouse, and Rat reactivity.

Source: BosterBio MTERF1 gene-info card — filtered to Western-blot-capable antibodies; each card shows that product's actual WB validation figure.