Recombinant Human WT1 protein, His & GST-tagged

Cat.No. : WT1-1402H
Product Overview : Recombinant Human WT1 aa. (Leu310~Leu449 fused with N-terminal His & GST tag was produced in E. coli cells.
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Description : This gene encodes a transcription factor that contains four zinc-finger motifs at the C-terminus and a proline/glutamine-rich DNA-binding domain at the N-terminus. It has an essential role in the normal development of the urogenital system, and it is mutated in a small subset of patients with Wilms tumor. This gene exhibits complex tissue-specific and polymorphic imprinting pattern, with biallelic, and monoallelic expression from the maternal and paternal alleles in different tissues. Multiple transcript variants have been described. In several variants, there is evidence for the use of a non-AUG (CUG) translation initiation codon upstream of, and in-frame with the first AUG. Authors of PMID:7926762 also provide evidence that WT1 mRNA undergoes RNA editing in human and rat, and that this process is tissue-restricted and developmentally regulated.
Source : E. coli
Species : Human
Tag : His&GST
Form : Freeze-dried powder
Molecular Mass : 47kDa as determined by SDS-PAGE reducing conditions.
Protein length : Leu310~Leu449
Endotoxin : <1.0EU per 1µg (determined by the LAL method)
Purity : >90%
Characteristic : The isoelectric point is 10.3.
Applications : Positive Control; Immunogen; SDS-PAGE; WB.
Stability : The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37°C for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition.
Storage : Avoid repeated freeze/thaw cycles. Store at 2-8°C for one month. Aliquot and store at -80°C for 12 months.
Concentration : 200μg/mL
Storage buffer : 100mM NaHCO3, 500mM NaCl, pH8.3, containing 1mM EDTA, 1mM DTT, 0.01% sarcosyl, 5% Trehalose and Proclin300.
Reconstitution : Reconstitute in 100mM NaHCO3, 500mM NaCl (pH8.3) to a concentration of 0.1-1.0 mg/mL. Do not vortex.
Gene Name : WT1 Wilms tumor 1 [ Homo sapiens (human) ]
Official Symbol : WT1
Synonyms : WT1; Wilms tumor 1; GUD; AWT1; WAGR; WT33; NPHS4; WIT-2; EWS-WT1; Wilms tumor protein; Wilms tumor protein isoform Ex4a(+)
Gene ID : 7490
mRNA Refseq : NM_000378.4
Protein Refseq : NP_000369.3
UniProt ID : P19544

Not For Human Consumption!

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10/10/2020

    It has been widely employed in protein electron microscopy structure analysis, where it has demonstrated remarkable efficacy.

    10/25/2019

      Broad applicability make it a valuable asset for a wide range of research endeavors.

      05/07/2017

        Researchers can rely on the WT1 Protein to deliver reliable and reproducible results, facilitating robust data interpretation and scientific advancements.

        Q&As (5)

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        What therapeutic strategies are being explored for cancers with abnormal WT1 expression? 05/25/2021

        Targeted therapies and immunotherapies aimed at inhibiting or modulating WT1 expression are being investigated for their potential in cancer treatment.

        In what other cancers is the WT1 protein targeted for diagnostic purposes? 09/04/2019

        Apart from Wilms' tumor, WT1 is examined in leukemia, mesothelioma, and some solid tumors as a diagnostic marker.

        Can WT1 be a target for personalized cancer therapy? 04/01/2019

        Yes, understanding the WT1 status in a patient's cancer can guide the development of personalized treatment plans, potentially improving outcomes.

        Are there any ongoing clinical trials focused on the WT1 protein and cancer? 02/09/2019

        Yes, there are several clinical trials exploring the role of WT1 as a therapeutic target and its potential in cancer treatment.

        How does the WT1 protein contribute to the prognosis of cancer patients? 10/23/2017

        High levels of WT1 expression are often associated with poor prognosis in various cancers, indicating a more aggressive disease course.

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