PA548425

Krt222 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PA548425-Each-of-1 In Stock ₹ 46,502.50

PA548425 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

Krt222

Classification

Polyclonal

Formulation

PBS with 0.09% sodium azide

Gene Accession No.

Q8CCX5, Q8N1A0

Gene Symbols

Krt222

Immunogen

KLH conjugated synthetic peptide between 222-250 amino acids from the C-terminal region of human KRT222P.

Quantity

400 μL

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG

Applications

Western Blot

Conjugate

Unconjugated

Gene

Krt222

Gene Alias

6330509G02Rik; KA21; keratin 222; keratin 222 pseudogene; keratin 222, type II; keratin-222; Keratin-222 pseudogene; keratin-like protein KRT222; Krt222; KRT222P

Host Species

Rabbit

Purification Method

Antigen affinity chromatography, Protein A

Regulatory Status

RUO

Gene ID (Entrez)

125113, 268481

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

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Description

  • Predicted to react with bovine based on sequence homology
  • KRT222, also known as KRT222P
  • KRT222 is a 295 amino acid protein belonging to the intermediate filament family
  • The gene encoding KRT222P has been listed as a pseudogene, however it has not been established that the protein is not translated, and is therefore treated as a protein coding gene
  • Existing as two alternatively spliced isoforms, the gene encoding KRT222P maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes
  • Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1
  • Tumor suppressor p53 is necessary for maintenance of cellular genetic integrity by moderating cell fate through DNA repair versus cell death
  • Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome
  • Like p53, BRCA1 is directly involved in DNA repair, though specifically it is recognized as a genetic determinant of early onset breast cancer and predisposition to cancers of the ovary, colon, prostate gland and fallopian tubes.