50-155-7851

UBAP2L/NICE4 Polyclonal Antibody, Bethyl Laboratories

Manufacturer: Bethyl Laboratories, Inc

Select a Size

Pack Size SKU Availability Price
Each of 1 50-155-7851-Each-of-1 In Stock ₹ 12,384.35

50-155-7851 - Each of 1

₹ 12,384.35

In Stock

Quantity

1

Base Price: ₹ 12,384.35

GST (18%): ₹ 2,229.183

Total Price: ₹ 14,613.533

Antigen

UBAP2L/NICE4

Classification

Polyclonal

Formulation

TBS with 0.1% BSA and 0.09% sodium azide

Gene Accession No.

Q14157

Gene Symbols

UBAP2L

Immunogen

Between 400 and 450

Quantity

20 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

Applications

Western Blot

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

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Description

  • The recommended shelf life for this product is 1 year from date of receipt
  • 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.