Recombinant Human ALKBH8 lysate
Cat.No. : | ALKBH8-18HCL |
Product Overview : | Over-expression cells lysed in RIPA buffer and lysate supplied in SDS loading buffer |
- Specification
- Gene Information
- Related Products
Source : | HEK 293 cells |
Species : | Human |
Molecular Mass : | 30793.7Da |
Recommended Usage : | WB |
Storage Instruction : | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
Gene Name : | ALKBH8 alkB, alkylation repair homolog 8 (E. coli) [ Homo sapiens ] |
Official Symbol : | ALKBH8 |
Synonyms : | ALKBH8; alkB, alkylation repair homolog 8 (E. coli); alkylated DNA repair protein alkB homolog 8; MGC10235; AlkB homologue 8; probable alpha-ketoglutarate-dependent dioxygenase ABH8; tRNA (carboxymethyluridine(34)-5-O)-methyltransferase ABH8; S-adenosyl-L-methionine-dependent tRNA methyltransferase ABH8; ABH8; FLJ38204; |
Gene ID : | 91801 |
mRNA Refseq : | NM_138775 |
Protein Refseq : | NP_620130 |
MIM : | 613306 |
UniProt ID : | Q96BT7 |
Chromosome Location : | 11q22.3 |
Function : | RNA binding; metal ion binding; methyltransferase activity; nucleotide binding; oxidoreductase activity; oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, 2-oxoglutarate as one donor, and incorporation of one atom each of oxygen into both donors; protein binding; tRNA (uracil) methyltransferase activity; transferase activity; |
Products Types
◆ Recombinant Protein | ||
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ALKBH8-1560M | Recombinant Mouse ALKBH8 Protein | +Inquiry |
ALKBH8-479H | Recombinant Human ALKBH8 Protein, GST-tagged | +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.
Inquiry
- Q&As
- Reviews
Q&As (16)
Ask a questionThe mutation of ALKBH8 gene is related to individual heredity, age, gender and so on.
Mutations in the ALKBH8 gene can be regulated and influenced by a healthy lifestyle.
There is currently no specific treatment for the ALKBH8 gene mutation, but treatments can be tailored to the symptoms that occur.
The ALKBH8 gene has been linked to breast cancer, neurological diseases and more.
Mutations in the ALKBH8 gene may affect the body's immunity, but the exact extent of the impact needs to be further studied.
The ALKBH8 gene may affect the immune system, but the specific mechanism needs to be further studied.
ALKBH8 gene is expressed in various tissues, including breast, ovary, kidney, brain and so on.
Mutations in the ALKBH8 gene may cause some genetic diseases.
Mutations in the ALKBH8 gene may lead to long-term health consequences that need to be studied further.
The expression of ALKBH8 gene may be related to cell apoptosis, DNA repair and other physiological processes.
The mutation of ALKBH8 gene may be inherited, and the specific inheritance mode needs to be further studied.
Mutations in the ALKBH8 gene can be diagnosed by methods such as gene sequencing.
The mutation of ALKBH8 gene may be related to environmental factors such as chemicals and radiation.
Mutation of ALKBH8 gene may cause damage to DNA repair, resulting in cell apoptosis obstruction, cell mutation and other problems.
Mutations in the ALKBH8 gene may affect fertility, but the exact extent needs to be further studied.
There is currently no specific cure for mutations in the ALKBH8 gene.
Customer Reviews (3)
Write a reviewGood stability and activity during long-term storage.
It is effective and safe in clinical treatment.
ALKBH8 is not structurally or functionally defective.
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