TFB1M Antibody, FITC conjugated

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Description

Key Functional Roles of TFB1M

TFB1M is a mitochondrial methyltransferase that dimethylates 12S rRNA at residues A1583 and A1584, critical for ribosomal small subunit assembly . It also regulates mitochondrial DNA transcription via interactions with POLRMT and TFAM .

Experimental Use Cases

  • Mitochondrial Ribosome Assembly Studies: Knockdown of TFB1M disrupts mitochondrial small subunit (28S) assembly, reducing ATP production and impairing mitochondrial protein synthesis .

  • Cancer Research: TFB1M overexpression in hepatocellular carcinoma (HCC) promotes aerobic glycolysis (Warburg effect) and metastasis by altering mitochondrial metabolism .

Recommended Dilutions

ApplicationDilution RangeValidated Cell Lines
Immunofluorescence1:400–1:1600HepG2 (human liver cancer)
Immunoprecipitation0.5–4.0 µg/1–3 mg lysateHepG2

Comparative Analysis of TFB1M Antibodies

The table below contrasts the FITC-conjugated TFB1M antibody with other commercially available variants:

Catalog No.ConjugateHostApplicationsReactivityKey Validation Data
ABIN7149948FITCRabbitIF, IHC, ELISA, WB*HumanEpitope: AA 59–194
ab236901NoneRabbitWB, IHC-P, ICC/IFHumanValidated in A549, HepG2 cells
16604-1-APNoneRabbitIP, IF/ICC, ELISAHumanIP-validated in HepG2 lysates

Research Findings Using TFB1M Antibodies

  • Mitochondrial Translation: Knockdown of TFB1M reduced puromycin incorporation into nascent mitochondrial proteins by 60%, confirming its role in translation .

  • Metabolic Reprogramming: TFB1M overexpression in HCC cells increased lactate production by 2.5-fold and decreased oxygen consumption by 40%, linking it to the Warburg effect .

Limitations and Considerations

  • Species Cross-Reactivity: Limited to human samples; non-human reactivity is untested .

  • Application Specificity: Optimal dilution must be empirically determined for untested applications (e.g., flow cytometry) .

Product Specs

Buffer
**Preservative:** 0.03% Proclin 300
**Constituents:** 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
Typically, we can ship your orders within 1-3 business days of receiving them. Delivery time may vary depending on the purchasing method or location. Please consult your local distributor for specific delivery timelines.
Synonyms
N'-adenosyl(rRNA) dimethyltransferase 1 antibody; CGI75 antibody; Dimethyladenosine transferase 1; mitochondrial antibody; h-mtTFB antibody; h-mtTFB1 antibody; hmtTFB antibody; hmtTFB1 antibody; hTFB1M antibody; Mitochondrial 12S rRNA dimethylase 1 antibody; Mitochondrial dimethyladenosine transferase 1 antibody; Mitochondrial transcription factor B1 antibody; mtTFB1 antibody; S-adenosylmethionine-6-N' antibody; Tfb1m antibody; TFB1M_HUMAN antibody; Transcription factor B1 mitochondrial antibody
Target Names
TFB1M
Uniprot No.

Target Background

Function
TFB1M (Transcription Factor B1, Mitochondrial) is an S-adenosyl-L-methionine-dependent methyltransferase that specifically dimethylates mitochondrial 12S rRNA at the conserved stem loop. It also plays a crucial role in the basal transcription of mitochondrial DNA, likely through its interaction with POLRMT and TFAM. Notably, TFB1M can stimulate transcription independently of its methyltransferase activity.
Gene References Into Functions
  1. Loss of TFB1M leads to mitochondrial dysfunction, resulting in impaired insulin secretion and diabetes. PMID: 24916378
  2. Deficiency in TFB1M and subsequent impaired mitochondrial function contribute significantly to the pathogenesis of type 2 diabetes. PMID: 21195351
  3. Endurance training has been shown to influence the mRNA levels of TFB1M and TFB2M. PMID: 19681768
  4. This transcription factor effectively activates the transcription of human mitochondrial DNA. PMID: 12068295
  5. Human mitochondrial transcription factor B1 (TFB1M) methylates ribosomal RNA at a conserved stem-loop. PMID: 12496758
  6. TFB1M interacts with the C-terminal activation region of h-mtTFA and stimulates transcription independently of its RNA methyltransferase activity. PMID: 12897151
  7. TFB1M is identified as a nuclear-encoded modifier gene for the phenotypic expression of the deafness-associated homoplasmic A1555G mutation in the mitochondrial 12S rRNA gene. PMID: 15110318
  8. Distinct, yet possibly coordinated functions of mtTFB1 and mtTFB2 in mitochondrial gene expression and biogenesis have been observed. PMID: 17557812
  9. Research suggests that DNA variants in TFB1M do not contribute to the risk of Parkinson's disease. PMID: 18980857
  10. A study examined the variation in TFAM, TFB1M, and TFB2M genes in cardiac hypertrophy. PMID: 19096125
  11. rRNA methyltransferase activity is essential for the induction of mitochondrial biogenesis by TFB1M, but not TFB2M. PMID: 19417006

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Database Links

HGNC: 17037

OMIM: 607033

KEGG: hsa:51106

STRING: 9606.ENSP00000356134

UniGene: Hs.279908

Involvement In Disease
Variations in TFB1M may influence the clinical expression of aminoglycoside-induced deafness caused by the A1555G mutation in the mitochondrial 12S rRNA.
Protein Families
Class I-like SAM-binding methyltransferase superfamily, rRNA adenine N(6)-methyltransferase family, KsgA subfamily
Subcellular Location
Mitochondrion.
Tissue Specificity
Ubiquitously expressed.

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