• Western blot analysis of extracts of various cell lines, using hnRNP C rabbit monoclonal antibody (STJ11102402) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% non-fat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 3s.
  • Confocal imaging of paraffin-embedded Human colon cancer using hnRNP C Rabbit monoclonal antibody (STJ11102402, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) ( dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). Objective: 40x. Perform high pressure antigen retrieval with 0. 01 M citrate buffer (pH 6. 0) prior to IF staining.
  • Immunofluorescence analysis of U-2 OS cells using hnRNP C rabbit monoclonal antibody (STJ11102402) at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.
  • Confocal imaging of U-2 OS cells using hnRNP C Rabbit monoclonal antibody (STJ11102402, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (dilution 1:500) (Red). The cells were counterstained with Alpha-Tubulin Mouse monoclonal antibody ( dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) antibody ( dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.
  • Western blot analysis of various lysates using hnRNP C Rabbit monoclonal antibody (STJ11102402) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (STJS000856) at 1:10000 dilution. Lysates/proteins: 25 Mu g per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 3s.

Anti-HNRNPC antibody (80-170) [S2MR] (STJ11102402)

SKU:
STJ11102402

£146.50 - £639.50
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Host: Rabbit
Applications: WB/IF
Reactivity: Human/Mouse
Note: STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Short Description: Rabbit monoclonal antibody anti-hnRNP C1 + C2 (80-170) is suitable for use in Western Blot and Immunofluorescence research applications.
Clonality: Monoclonal
Clone ID: S2MR
Conjugation: Unconjugated
Isotype: IgG
Formulation: PBS with 0.02% Sodium Azide, 0.05% BSA, 50% Glycerol, pH7.3.
Purification: Affinity purification
Dilution Range: WB 1:500-1:2000
IF/ICC 1:50-1:200
Storage Instruction: Store at-20°C for up to 1 year from the date of receipt, and avoid repeat freeze-thaw cycles.
Gene Symbol: HNRNPC
Gene ID: 3183
Uniprot ID: HNRPC_HUMAN
Immunogen Region: 80-170
Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 80-170 of human hnRNP C (P07910).
Immunogen Sequence: LDINLAAEPKVNRGKAGVKR SAAEMYGSVTEHPSPSPLLS SSFDLDYDFQRDYYDRMYSY PARVPPPPPIARAVVPSKRQ RVSGNTSRRGK
Post Translational Modifications Phosphorylated on Ser-260 and Ser-299 in resting cells. Phosphorylated on Ser-253 and on 1 serine residue in the poly-Ser stretch at position 238 in response to hydrogen peroxide. Sumoylated. Sumoylation reduces affinity for mRNA.
Function Binds pre-mRNA and nucleates the assembly of 40S hnRNP particles. Interacts with poly-U tracts in the 3'-UTR or 5'-UTR of mRNA and modulates the stability and the level of translation of bound mRNA molecules. Single HNRNPC tetramers bind 230-240 nucleotides. Trimers of HNRNPC tetramers bind 700 nucleotides. May play a role in the early steps of spliceosome assembly and pre-mRNA splicing. N6-methyladenosine (m6A) has been shown to alter the local structure in mRNAs and long non-coding RNAs (lncRNAs) via a mechanism named 'm(6)A-switch', facilitating binding of HNRNPC, leading to regulation of mRNA splicing.
Protein Name Heterogeneous Nuclear Ribonucleoproteins C1/C2
Hnrnp C1/C2
Database Links Reactome: R-HSA-4570464
Reactome: R-HSA-72163
Reactome: R-HSA-72203
Reactome: R-HSA-9013418
Reactome: R-HSA-9013422
Cellular Localisation Nucleus
Component Of Ribonucleosomes
Alternative Antibody Names Anti-Heterogeneous Nuclear Ribonucleoproteins C1/C2 antibody
Anti-Hnrnp C1/C2 antibody
Anti-HNRNPC antibody
Anti-HNRPC antibody

Information sourced from Uniprot.org

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