
Immunohistochemical analysis of paraffin-embedded Cal27 xenograft, using BLM(GTX101303) antibody at 1:100 dilution.
Antigen Retrieval: Trilogy? (EDTA based, pH 8.0) buffer, 15min
BLM antibody [C3], C-term
GTX101303
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetBLM
Overview
- SupplierGeneTex
- Product NameBLM antibody [C3], C-term
- Delivery Days Customer9
- Application Supplier NoteWB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
- CertificationResearch Use Only
- ClonalityPolyclonal
- Concentration1.34 mg/ml
- ConjugateUnconjugated
- Gene ID641
- Target nameBLM
- Target descriptionBLM RecQ like helicase
- Target synonymsBS, MGRISCE1, RECQ2, RECQL2, RECQL3, recQ-like DNA helicase BLM, Bloom syndrome RecQ like helicase, Bloom syndrome, RecQ helicase-like, DNA 3'-5' helicase BLM, DNA helicase, RecQ-like type 2, bloom syndrome protein, recQ protein-like 3
- HostRabbit
- IsotypeIgG
- Protein IDP54132
- Protein NameRecQ-like DNA helicase BLM
- Scientific DescriptionThe Bloom syndrome gene product is related to the RecQ subset of DExH box-containing DNA helicases and has both DNA-stimulated ATPase and ATP-dependent DNA helicase activities. Mutations causing Bloom syndrome delete or alter helicase motifs and may disable the 3-5 helicase activity. The normal protein may act to suppress inappropriate recombination. [provided by RefSeq]
- ReactivityHuman
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203
References
- Truong LN, Li Y, Shi LZ, et al. Microhomology-mediated End Joining and Homologous Recombination share the initial end resection step to repair DNA double-strand breaks in mammalian cells. Proc Natl Acad Sci U S A. 2013,110(19):7720-5. doi: 10.1073/pnas.1213431110Read this paper
![Untreated (–) and treated (+) THP-1 cells were untreated or treated with 10 ng/ml PMA for 24 hrs (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with BLM antibody [C3], C-term (GTX101303) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced. Untreated (–) and treated (+) THP-1 cells were untreated or treated with 10 ng/ml PMA for 24 hrs (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with BLM antibody [C3], C-term (GTX101303) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](https://www.genetex.com/upload/website/prouct_img/normal/GTX101303/GTX101303_44489_20211217_WB_treatment_PMA_w_23060100_595.webp)
![BLM antibody [C3], C-term detects BLM protein at nucleus by immunofluorescent analysis. Sample: A431 cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: BLM protein stained by BLM antibody [C3], C-term (GTX101303) diluted at 1:200. Blue: Hoechst 33342 staining. BLM antibody [C3], C-term detects BLM protein at nucleus by immunofluorescent analysis. Sample: A431 cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: BLM protein stained by BLM antibody [C3], C-term (GTX101303) diluted at 1:200. Blue: Hoechst 33342 staining.](https://www.genetex.com/upload/website/prouct_img/normal/GTX101303/GTX101303_39862_20160525_IFA_w_23060100_140.webp)
![Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with BLM antibody [C3], C-term (GTX101303) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program. Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with BLM antibody [C3], C-term (GTX101303) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program.](https://www.genetex.com/upload/website/prouct_img/normal/GTX101303/GTX101303_44489_20240202_WB_TPM_watermark_24021917_826.webp)

![Untreated (–) and treated (+) THP-1 whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with BLM antibody [HL2771] (GTX639636) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.](https://www.genetex.com/upload/website/prouct_img/normal/GTX639636/GTX639636_T-45299_20240126_WB_treatment_PMA_24013018_522.webp)



