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AB229238

Anti-HCC1 antibody

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(1 Publication)

Rabbit Polyclonal HCC1 antibody. Suitable for WB and reacts with Human, Mouse samples. Cited in 1 publication. Immunogen corresponding to Recombinant Fragment Protein within Human RBM39.

View Alternative Names

HCC1, RNPC2, RBM39, RNA-binding protein 39, CAPER alpha, Hepatocellular carcinoma protein 1, RNA-binding motif protein 39, RNA-binding region-containing protein 2, Splicing factor HCC1, CAPERalpha

2 Images
Western blot - Anti-HCC1 antibody (AB229238)
  • WB

Supplier Data

Western blot - Anti-HCC1 antibody (AB229238)

7.5% SDS-PAGE gel.

All lanes:

Western blot - Anti-HCC1 antibody (ab229238) at 1/1000 dilution

All lanes:

A431 (human epidermoid carcinoma cell line) whole cell lysate at 30 µg

Predicted band size: 59 kDa

false

Western blot - Anti-HCC1 antibody (AB229238)
  • WB

Supplier Data

Western blot - Anti-HCC1 antibody (AB229238)

7.5% SDS-PAGE gel.

All lanes:

Western blot - Anti-HCC1 antibody (ab229238) at 1/1000 dilution

Lane 1:

NIH/3T3 (mouse embryo fibroblast cell line) whole cell lysate at 30 µg

Lane 2:

JC whole cell lysate at 30 µg

Predicted band size: 59 kDa

false

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Reacts with

Mouse, Human

Applications

WB

applications

Immunogen

Recombinant Fragment Protein within Human RBM39. The exact immunogen used to generate this antibody is proprietary information.

Q14498

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "WB" : {"fullname" : "Western blot", "shortname":"WB"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1/500 - 1/3000", "WB-species-notes": "<p></p>" }, "Mouse": { "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1/500 - 1/3000", "WB-species-notes": "<p></p>" }, "Rat": { "WB-species-checked": "predicted", "WB-species-dilution-info": "", "WB-species-notes": "" }, "Cow": { "WB-species-checked": "predicted", "WB-species-dilution-info": "", "WB-species-notes": "" }, "Rabbit": { "WB-species-checked": "predicted", "WB-species-dilution-info": "", "WB-species-notes": "" } } }

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Immunogen
Storage buffer
pH: 7 Preservative: 0.01% Thimerosal (merthiolate) Constituents: PBS, 20% Glycerol (glycerin, glycerine), 1% BSA
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

The target HCC1 also known as HkCdc4 is a protein with a molecular mass of approximately 44 kDa. It plays a role in cell cycle regulation by acting as a regulator of cyclin levels. HCC1 is widely expressed in numerous tissues with notable expression in testis colon and leukocytes. It functions primarily within the nucleus where it impacts various cellular processes including transcription and mitosis.
Biological function summary

HCC1 influences cell division and growth regulation as part of a larger protein complex. It interacts with components such as cyclins and CDKs to ensure proper progression through the cell cycle. The protein modulates the stability and degradation of specific cyclins therefore contributing to orderly cell cycle transitions. These activities position HCC1 as an important player in maintaining chromosomal stability further integrating it with mitotic checkpoint machinery.

Pathways

The interaction of HCC1 integrates into pivotal pathways like the cell cycle regulatory pathway and the Wnt signaling pathway. The cell cycle pathway involves interactions with CDKs and cyclins affecting checkpoints and transitions. In the Wnt signaling context HCC1 interacts with proteins like β-catenin helping to harmonize cellular proliferation signals and the cell cycle's momentum. These interactions indicate the adaptability of HCC1 within complex pathway networks essential for cellular proliferation and signaling.

Aberrant HCC1 activity links to various types of cancer and reproductive disorders. HCC1 dysfunction often associates with hepatocellular carcinoma due to its role in cell cycle misregulation. This dysfunction also relates to disorders such as testicular dysgenesis syndrome where abnormal expression of HCC1 may contribute to improper developmental signaling. In these disorders HCC1 may work in conjunction with proteins like p53 further justifying its influence in processes that regulate cell growth and apoptosis.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

RNA-binding protein that acts as a pre-mRNA splicing factor (PubMed : 15694343, PubMed : 24795046, PubMed : 28302793, PubMed : 28437394, PubMed : 31271494). Acts by promoting exon inclusion via regulation of exon cassette splicing (PubMed : 31271494). Also acts as a transcriptional coactivator for steroid nuclear receptors ESR1/ER-alpha and ESR2/ER-beta, and JUN/AP-1, independently of the pre-mRNA splicing factor activity (By similarity).
See full target information RBM39

Publications (1)

Recent publications for all applications. Explore the full list and refine your search

Frontiers in pharmacology 13:857774 PubMed35592424

2022

Comprehensive Analysis of the Potential Immune-Related Biomarker ATG101 that Regulates Apoptosis of Cholangiocarcinoma Cells After Photodynamic Therapy.

Applications

Unspecified application

Species

Unspecified reactive species

Zi-Jian Zhang,Kun-Peng Wang,Yun-Peng Huang,Chong Jin,Hao Jiang,Li Xiong,Zhao-Yi Chen,Yu Wen,Zhong-Tao Liu,Jing-Gang Mo
View all publications

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