Price range: $268.00 through $328.00
Background:
WT1, located on chromosome 11p13, is a tumor suppressor gene, which mainly plays a role in the development of genitourinary organs. It was positive in ovarian serous carcinoma, peritoneal serous carcinoma, ovarian metastatic carcinoma, 50% of ovarian endometrial carcinoma, posterior renal adenoma, most malignant mesothelioma and sex cord stromal tumor.
| Target | Wilms' Tumor 1 |
| Reactivity | Human, Mouse, Rat, Pig |
| Applications | IHC, WB, IF, ELISA |
| MW(Calculated) | 55kD |
| MW(Observed) | 55kD |
| Host Species | Mouse |
| Isotype | IgG2b,Kappa |
| Conjugate/Modification | Unmodified |
| Modification | |
| Recommended Dilution Ratio | IHC 1:200-1000; WB 1:500-2000; IF 1:100-500; ELISA 1:1000-5000 / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#YS0004) |
| Formulation | PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA |
| Source | |
| Purification | Recombinant Antibody expressed in animal component-free (ACF) media, purified via Protein G affinity chromatography. |
| Purity | |
| Storage | -15°C to -25°C/1 year(Do not lower than -25°C) |
| Concentration | |
| Clonality | Monoclonal |
| Clone Number | ABT-WT1 |
| Immunogen | Synthesized peptide derived from human Wilms' Tumor 1(WT1) AA range: 350-449 |
| Sequence | |
| Specificity | The antibody can specifically recognize human WT1 protein. |
| Gene Name | WT1 |
| Protein Name | Wilms tumor protein (WT33) |
| Other Name | WIT 2; / WT 1; / AWT1; / FWT1; / GUD; / NPHS4; / WAGR; / Wilms tumor 1; / Wilms Tumor; / Wilms tumor protein; / Wilms' tumor gene; / Wilms' tumor protein; / WIT2; / WT; / WT1; / WT1_HUMAN; / WT33 |
| Species | Human |
| Gene ID-1 | 7490 |
| Uniprot | P19544 |
| Species.1 | |
| Gene ID-2 | |
| Uniprot.1 | |
| Species.2 | |
| Gene ID-3 | |
| Uniprot.2 | |
| Organism-4 | |
| Gene ID-4 | |
| SwissProt-4 | |
| Background | WT1, located on chromosome 11p13, is a tumor suppressor gene, which mainly plays a role in the development of genitourinary organs. It was positive in ovarian serous carcinoma, peritoneal serous carcinoma, ovarian metastatic carcinoma, 50% of ovarian endometrial carcinoma, posterior renal adenoma, most malignant mesothelioma and sex cord stromal tumor. |
| Cellular Localization | Nuclear |
| Tissue Expression | Expressed in the kidney and a subset of hematopoietic cells. |
| Signaling_pathway | Human Diseases >> Cancer: overview >> Transcriptional misregulation in cancer |
| Research Areas | >>Transcriptional misregulation in cancer |
| Function | Disease:A chromosomal aberration involving WT1 may be a cause of desmoplastic small round cell tumor (DSRCT). Translocation t(11; 22)(p13; q12) with EWSR1.,Disease:Defects in WT1 are a cause of hypospadias. Hypospadias is a common malformation in which the urethra opens on the ventral side of the penis. It is considered a complex disorder with both genetic and environmental factors involved in the pathogenesis. Hypospadias can occur alone on an apparently multifactorial basis or as part of syndromes.,Disease:Defects in WT1 are a cause of Meacham syndrome [MIM:608978]. Meacham syndrome is a rare sporadically occurring multiple malformation syndrome characterized by male pseudohermaphroditism with abnormal internal female genitalia comprising a uterus and double or septate vagina, complex congenital heart defect and diaphragmatic abnormalities.,Disease:Defects in WT1 are a cause of Wilms tumor--aniridia--genitourinary anomalies--mental retardation syndrome (WAGR syndrome) [MIM:194072].,Disease:Defects in WT1 are the cause of Denys-Drash syndrome (DDS) [MIM:194080]. DDS is a typical nephropathy characterized by diffuse mesangial sclerosis, genital abnormalities, and/or Wilms tumor. There is phenotypic overlap with WAGR syndrome and Frasier syndrome. Inheritance is autosomal dominant, but most cases are sporadic.,Disease:Defects in WT1 are the cause of Frasier syndrome (FS) [MIM:136680]. FS is characterized by a slowly progressing nephropathy leading to renal failure in adolescence or early adulthood, male pseudohermaphroditism, and no Wilms tumor. As for histological findings of the kidneys, focal glomerular sclerosis is often observed. There is phenotypic overlap with Denys-Drash syndrome. Inheritance is autosomal dominant.,Disease:Defects in WT1 are the cause of isolated diffuse mesangial sclerosis (IDMS) [MIM:256370]. IDMS is an early-onset nephrotic syndrome occurring in the absence of other abnormalities and resulting in renal failure. Inheritance is autosomal recessive.,Disease:Defects in WT1 are the cause of Wilms tumor 1 (WT1) [MIM:194070]. WT is an embryonal malignancy of the kidney that affects approximately 1 in 10'000 infants and young children. It occurs both in sporadic and hereditary forms.,Function:Potential role in transcriptional regulation. Recognizes and binds to the DNA sequence 5'-CGCCCCCGC-3'.,similarity:Belongs to the EGR C2H2-type zinc-finger protein family.,similarity:Contains 4 C2H2-type zinc fingers.,subunit:Interacts with WTIP (By similarity). Interacts with ZNF224 via the zinc-finger region. Interacts with WTAP and SRY.,tissue specificity:Expressed in the kidney and a subset of hematopoietic cells., |
| RRID |
