Tested Applications
| Positive WB detected in | Jurkat cells, NIH/3T3 cells |
| Positive IHC detected in | rat lung tissue, rat stomach tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
Recommended dilution
| Application | Dilution |
|---|---|
| Western Blot (WB) | WB : 1:500-1:2000 |
| Immunohistochemistry (IHC) | IHC : 1:500-1:2000 |
| It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
| Sample-dependent, Check data in validation data gallery. | |
Product Information
24949-1-AP targets HIC1 in WB, IHC, IF, ELISA applications and shows reactivity with human, mouse samples.
| Tested Reactivity | human, mouse |
| Cited Reactivity | human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen |
CatNo: Ag21849 Product name: Recombinant human HIC1 protein Source: e coli.-derived, PGEX-4T Tag: GST Domain: 89-408 aa of BC157027 Sequence: DGAEAAAAAAVAPGAEPSLGAVLAAASYLQIPDLVALCKKRLKRHGKYCHLRGGGGGGGGYAPYGRPGRGLRAATPVIQACYPSPVGPPPPPAAEPPSGPEAAVNTHCAELYASGPGPAAALCASERRCSPLCGLDLSKKSPPGSAAPERPLAERELPPRPDSPPSAGPAAYKEPPLALPSLPPLPFQKLEEAAPPSDPFRGGSGSPGPEPPGRPDGPSLLYRWMKHEPGLGSYGDELGRERGSPSERCEERGGDAAVSPGGPPLGLAPPPRYPGSLDGPGAGGDGDDYKSSSEETGSSEDPSPPGGHLEGYPCPHLAYG Predict reactive species |
| Full Name | hypermethylated in cancer 1 |
| Calculated Molecular Weight | 714 aa, 75 kDa |
| Observed Molecular Weight | 65-70 kDa |
| GenBank Accession Number | BC157027 |
| Gene Symbol | HIC1 |
| Gene ID (NCBI) | 3090 |
| RRID | AB_2879816 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Purification Method | Antigen affinity purification |
| UNIPROT ID | Q14526 |
| Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol, pH 7.3. |
| Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA. |
Protocols
| Product Specific Protocols | |
|---|---|
| IHC protocol for HIC1 antibody 24949-1-AP | Download protocol |
| WB protocol for HIC1 antibody 24949-1-AP | Download protocol |
| Standard Protocols | |
|---|---|
| Click here to view our Standard Protocols |
Publications
What published studies show
The HIC1 Polyclonal antibody (Cat# 24949-1-AP) has 5 citations published in Advanced Science, Frontiers in Immunology, Cancer Cell International, Frontiers in Cell and Developmental Biology, and Digestive Diseases and Sciences. The research fields span gastric cancer pyroptosis, ferroptosis-related immunotherapy prediction, bladder cancer progression, ovarian cancer diagnosis, and acute pancreatitis.
| Species | Application | Title |
|---|---|---|
Adv Sci (Weinh) HIC1 suppresses Tumor Progression and Enhances CD8+ T Cells Infiltration Through Promoting GSDMD-induced Pyroptosis in Gastric Cancer | ||
Cancer Cell Int ZBTB7A, a miR-144-3p targeted gene, accelerates bladder cancer progression via downregulating HIC1 expression. | ||
Front Immunol Ferroptosis-related gene HIC1 in the prediction of the prognosis and immunotherapeutic efficacy with immunological activity | ||
Front Cell Dev Biol Integrated Analysis of Ferroptosis-Related Biomarker Signatures to Improve the Diagnosis and Prognosis Prediction of Ovarian Cancer. | ||
Dig Dis Sci Mechanistic Investigation of FBXW11-Mediated Ubiquitination and Degradation of HIC1 in Regulating IRF1 Transcription and Accelerating Acute Pancreatitis Progression.
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Reviews
What customers say
One reviewer used this antibody at a 1/300 dilution for immunofluorescence staining of mouse embryo fibroblasts and reported excellent results, giving it a perfect 5-star rating. The user described the staining performance as "amazing," indicating strong satisfaction with the product's specificity and signal quality in this application.
The reviews below have been submitted by verified Proteintech customers who received an incentive for providing their feedback.
Shazia (Verified Customer) (08-25-2025) | I used it to stain fibroblasts and it worked amazingly.
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