Recombinant Rat Galt protein, His & T7-tagged
Cat.No. : | Galt-1613R |
Product Overview : | Recombinant Rat Galt aa. (Met1~Ala379 (Accession # P43424)) fused with N-terminal His & T7 tag was produced in E. coli cells. |
- Specification
- Gene Information
- Related Products
Source : | E. coli |
Species : | Rat |
Tag : | His & T7 |
Form : | Freeze-dried powder |
Molecular Mass : | Predicted Molecular Mass: 47.0kDa |
Protein length : | Met1~Ala379 (Accession # P43424) |
Endotoxin : | <1.0EU per 1ug (determined by the LAL method) |
Purity : | >95% |
Applications : | SDS-PAGE; WB; ELISA; IP. |
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. |
Storage buffer : | Supplied as lyophilized form in PBS, pH7.4, containing 5% trehalose, 0.01% sarcosyl. |
Reconstitution : | Reconstitute in sterile PBS, pH7.2-pH7.4. |
Isoelectric Point : | 6.1 |
Gene Name : | Galt galactose-1-phosphate uridylyltransferase [ Rattus norvegicus (Norway rat) ] |
Official Symbol : | Galt |
Synonyms : | Galt; galactose-1-phosphate uridylyltransferase; galactose-1-phosphate uridylyltransferase; UDP-glucose--hexose-1-phosphate uridylyltransferase; gal-1-P uridylyltransferase; galactose-1-phosphate uridyl transferase |
Gene ID : | 298003 |
mRNA Refseq : | NM_001013089.2 |
Protein Refseq : | NP_001013107.1 |
UniProt ID : | P43424 |
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◆ Native Protein | ||
GALT-10 | Active Native Streptoverticillium mobaraense | +Inquiry |
◆ Lysates | ||
GALT-6026HCL | Recombinant Human GALT 293 Cell Lysate | +Inquiry |
Related Gene
For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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Q&As (5)
Ask a questionTreatment for GALT deficiency involves a strict lactose-free diet, which means avoiding milk, dairy products, and other foods containing galactose.
Individuals with GALT deficiency are recommended to avoid galactose-containing foods, and dietary supplementation with essential nutrients may be necessary.
Yes, if left untreated, GALT deficiency can lead to long-term complications such as liver damage, cognitive impairment, and reproductive issues.
Yes, GALT enzyme activity levels can be measured in the blood to diagnose GALT deficiency.
Symptoms of galactosemia include jaundice, poor feeding, vomiting, liver enlargement, and failure to thrive in infants. In older children and adults, symptoms may include cognitive impairment, speech difficulties, and ovarian insufficiency in females.
Customer Reviews (3)
Write a reviewThe GALT Protein is an exceptional product that fully meets my experimental needs.
Its versatility and reliability make it a top choice for researchers in various fields.
The GALT Protein's adaptability has significantly expanded the scope of my investigations and broadened the possibilities for my research.
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