Recombinant Mouse ALMS1 Protein, His (Fc)-Avi-tagged
Cat.No. : | ALMS1-480M |
Product Overview : | Recombinant Mouse ALMS1 with His (Fc)-Avi tag was expressed and purified |
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Source : | HEK293 |
Species : | Mouse |
Tag : | His (Fc)-Avi |
Endotoxin : | < 1.0 EU per μg of the protein as determined by the LAL method |
Purity : | ≥85% by SDS-PAGE |
Stability : | Stable for at least 6 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Storage : | For long term storage, aliquot and store at -20 to -80 centigrade. Avoid repeated freezing and thawing cycles. |
Storage Buffer : | PBS buffer |
Gene Name : | Alms1 Alstrom syndrome 1 [ Mus musculus ] |
Official Symbol : | ALMS1 |
Gene ID : | 236266 |
mRNA Refseq : | NM_145223.2 |
Protein Refseq : | NP_660258.2 |
UniProt ID : | Q8K4E0 |
Products Types
◆ Recombinant Protein | ||
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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 (14)
Ask a questionThe ALMS1 gene is expressed in several tissues and organs, including the retina, cerebral cortex, small intestine, kidney, and pancreas.
Alstrom syndrome is an autosomal recessive disorder caused by a mutation in the ALMS1 gene.
No studies have shown that ALMS1 mutations are associated with cancer.
Mutations in the ALMS1 gene may lead to changes in the structure or function of the ALMS1 protein, which may affect its role in the cell as well as the metabolism and signaling processes of the entire cell.
There are treatments that address the symptoms of Alstrom syndrome, including vision rehabilitation training, diabetes treatment, and hearing tests.
The ALMS1 gene encodes the ALMS1 protein, the function of which is not fully understood.
Yes, some research suggests that the ALMS1 gene may also have a role in nervous system development.
Yes, there is a great diversity of ALMS1 mutations.
There are few studies on the relationship between ALMS1 gene mutation and congenital heart disease, and there is no clear conclusion at present.
Some studies suggest that ALMS1 gene mutations may be associated with autoimmune diseases, rheumatoid arthritis, etc.
Mutations in the ALMS1 gene may affect intellectual development, but the extent of the effect is less certain.
There is currently no gene therapy for the ALMS1 gene mutation.
Mutations in the ALMS1 gene can cause Alstrom syndrome, which has symptoms including early blindness, obesity, diabetes, deafness and more.
Yes, because Alstrom syndrome is an autosomal recessive disorder, the ALMS1 gene mutation may be passed on to the next generation.
Customer Reviews (4)
Write a reviewGood stability under different temperature and humidity conditions.
The effect of chemical modification, such as PEGylation or glycosylation, is small.
Accurate localization and function in cells.
ALMS1 was effective in removing impurities during purification.
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