ALMS1P
| Species | Cat.# | Product name | Source (Host) | Tag | Protein Length | Price |
|---|---|---|---|---|---|---|
| Human | ALMS1P-4700HCL | Recombinant Human LOC200420 293 Cell Lysate | HEK293 | N/A |
|
ALMS1P involved in several pathways and played different roles in them. We selected most pathways ALMS1P participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with ALMS1P were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name | Pathway Related Protein |
|---|
ALMS1P has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by ALMS1P itself. We selected most functions ALMS1P had, and list some proteins which have the same functions with ALMS1P. You can find most of the proteins on our site.
| Function | Related Protein |
|---|
ALMS1P has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with ALMS1P here. Most of them are supplied by our site. Hope this information will be useful for your research of ALMS1P.
- Q&As
- Reviews
Q&As (13)
Ask a questionALMS1P mainly presents with vision loss, hearing loss, obesity, diabetes, cardiovascular disease and other symptoms, and may also be accompanied by abnormalities of the urinary system and reproductive system.
The diagnosis of ALMS1P requires many professional examinations such as gene sequencing, eye examination, hearing examination and cardiac ultrasound.
This is a rare disease with an incidence of about 1-10 per million people, which varies by region and ethnicity.
ALMS1P is strongly associated with obesity and is also a risk factor for complications such as diabetes.
At present, the pathogenesis of ALMS1P is not fully understood, and it may be related to the abnormality of cell metabolism related pathways.
ALMS1P gene mutations may lead to cardiac dysfunctions such as cardiac hypertrophy, atrial dilation, and atrial tachycardia.
It may cause abnormal development of the reproductive system, irregular menstruation, polycystic ovary syndrome and other problems.
At present, the treatment methods of ALMS1P are mainly symptomatic treatment, such as vision correction, hearing aid, insulin therapy, etc., and more effective drugs and treatment methods need to be found in clinical practice.
This gene mutation mainly affects many biological pathways such as cell metabolism, cytokine signaling pathway, protein translation and delivery.
Mutations in the ALMS1P gene may affect the stroma and cellular structure of the retina, which can lead to symptoms such as vision loss and retinal atrophy.
Mutations in the ALMS1P gene may affect the stroma and cellular structure of the retina, which can lead to symptoms such as vision loss and retinal atrophy.
The prognosis of ALMS1P varies greatly from individual to individual, and some patients may have serious consequences such as heart failure, but there are some cases of good performance.
It is an autosomal recessive disorder that requires mutations in two genes to manifest.
Customer Reviews (3)
Write a reviewALMS1P was able to form a stable micellar structure.
The binding affinity and affinity constant to the target were high.
ALMS1P showed significant antibacterial activity and bactericidal effect against bacteria.
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