PA549924
CYP4X1 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PA549924-Each-of-1 | In Stock | ₹ 47,036.50 |
PA549924 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 47,036.50
GST (18%): ₹ 8,466.57
Total Price: ₹ 55,503.07
Antigen
CYP4X1
Classification
Polyclonal
Conjugate
Unconjugated
Gene
CYP4X1
Gene Alias
A230025G20; CP4X1; CYP_a; Cyp4a28-ps; Cyp4x1; CYPIVX1; cytochrome P450 4X1; cytochrome P450 family 4 subfamily X member 1; cytochrome P450, 4x1; cytochrome P450, family 4, subfamily X, polypeptide 1; EC 1.14.14.1; PRO4404; UNQ1929; UNQ1929/PRO4404
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
260293
Content And Storage
-20°C
Form
Liquid
Applications
Immunohistochemistry (Paraffin), Western Blot
Concentration
1 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
Gene Accession No.
Q8N118
Gene Symbols
CYP4X1
Immunogen
Synthesized peptide derived from internal of human Cytochrome P450 4X1.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- The antibody detects endogenous levels of total CYP4X1 protein
- Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome
- There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1
- Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A
- When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs
- The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration
- The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis
- Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1
- A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia
- Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma
- The CYP4X1 gene product has been provisionally designated CYP4X1 pending further characterization.