Recombinant Human ALKBH8 Protein, GST-tagged
Cat.No. : | ALKBH8-479H |
Product Overview : | Human ALKBH8 full-length ORF ( NP_620130.1, 1 a.a. - 238 a.a.) recombinant protein with GST-tag at N-terminal. |
- Specification
- Gene Information
- Related Products
Description : | ALKBH8 (AlkB Homolog 8, TRNA Methyltransferase) is a Protein Coding gene. Among its related pathways are tRNA processing and Gene Expression. GO annotations related to this gene include nucleic acid binding and nucleotide binding. An important paralog of this gene is KIAA1456. |
Source : | Wheat Germ |
Species : | Human |
Tag : | GST |
Molecular Mass : | 53.8 kDa |
AA Sequence : | MDSNHQSNYKLSKTEKKFLRKQIKA KHTLLRHEGIETVSYATQSLVVANG GLGNGVSRNQLLPVLEKCGLVDALL MPPNKPYSFARYRTTEESKRAYVTL NGKEVVDDLGQKITLYLNFVEKVQW KELRPQALPPGLMVVEEIISSEEEK MLLESVDWTEDTDNQNSQKSLKHRR VKHFGYEFHYENNNVDKDKPLSGGL PDICESFLEKWLRKGYIKHKPDQMT INQYEPGQDCHGF |
Applications : | Enzyme-linked Immunoabsorbent Assay; Western Blot (Recombinant protein); Antibody Production; Protein Array |
Notes : | Best use within three months from the date of receipt of this protein. |
Storage : | Store at -80 centigrade. Aliquot to avoid repeated freezing and thawing. |
Storage Buffer : | 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer. |
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 |
Products Types
◆ Recombinant Protein | ||
ALKBH8-479M | Recombinant Mouse ALKBH8 Protein, His (Fc)-Avi-tagged | +Inquiry |
Alkbh8-1603M | Recombinant Mouse Alkbh8 Protein, Myc/DDK-tagged | +Inquiry |
ALKBH8-322H | Recombinant Human ALKBH8 Protein, His (Fc)-Avi-tagged | +Inquiry |
ALKBH8-1560M | Recombinant Mouse ALKBH8 Protein | +Inquiry |
ALKBH8-3274B | Recombinant Bovine ALKBH8, His-tagged | +Inquiry |
◆ Lysates | ||
ALKBH8-18HCL | Recombinant Human ALKBH8 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 (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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