50-155-7852
UBAP2L/NICE4 Rabbit anti-Human, Polyclonal, Bethyl Laboratories
Manufacturer: Bethyl Laboratories, Inc
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | 50-155-7852-Each-of-1 | In Stock | ₹ 43,546.81 |
50-155-7852 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 43,546.81
GST (18%): ₹ 7,838.426
Total Price: ₹ 51,385.236
Antigen
UBAP2L/NICE4
Classification
Polyclonal
Conjugate
Unconjugated
Gene
UBAP2L
Gene Alias
Ubiquitin-associated protein 2-like, Protein NICE-4, KIAA0144, NICE4
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
9898
Content And Storage
4° C
Form
Liquid
Applications
Immunoprecipitation, Western Blot
Concentration
1 mg/ml
Formulation
phosphate, tris citrate with 0.09% sodium azide; pH 7-8
Gene Accession No.
Q14157
Gene Symbols
UBAP2L
Immunogen
Between 1025 and C-term
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- The recommended shelf life for this product is 1 year from date of receipt
- Based on 100% sequence identity, this antibody is predicted to react with Mouse NICE4, also known as UBAP2L (Ubiquitin-associated protein 2-like) orKIAA0144, is a 1,087 amino acid protein that is ubiquitously expressed
- Phosphorylated upon DNA damage, NICE4 contains one UBA domain and is expressed as 4 isoforms produced by alternative splicing events
- The gene that encodes NICE4 maps to human chromosome 1
- 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.