50-155-7854

UBAP2L/NICE4 Polyclonal Antibody, Bethyl Laboratories

Manufacturer: Bethyl Laboratories, Inc

Select a Size

Pack Size SKU Availability Price
Each of 1 50-155-7854-Each-of-1 In Stock ₹ 12,384.35

50-155-7854 - 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 1025 and C-term

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
  • 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.