PA549987

DDX19B Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PA549987-Each-of-1 In Stock ₹ 46,502.50

PA549987 - 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

DDX19B

Classification

Polyclonal

Conjugate

Unconjugated

Gene

DDX19B

Gene Alias

2810457M08Rik; 4921519L13Rik; ATP-dependent RNA helicase DDX19; ATP-dependent RNA helicase DDX19B; AW260119; DBP5; DDX19; Ddx19b; DEAD (Asp-Glu-Ala-As) box polypeptide 19B; DEAD (Asp-Glu-Ala-Asp) box polypeptide 19b; DEAD box protein 19B; DEAD box RNA helicase DEAD5; DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 19 (Dbp5, yeast, homolog); DEAD-box helicase 19B; DEAD-box protein 5; DEAD-box RNA helicase DEAD5; RNAh; TDBP; Unknown (protein for MGC:134354); yeast Dbp5 homolog; Zd10a; zinc responsive protein Zd10A

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

11269, 234733

Content And Storage

-20°C

Form

Liquid

Applications

Western Blot

Concentration

1 mg/mL

Formulation

PBS with 50% glycerol and 0.02% sodium azide; pH 7.4

Gene Accession No.

Q9UMR2

Gene Symbols

DDX19B

Immunogen

Synthesized peptide derived from internal of human DDX19B.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG

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Description

  • The antibody detects endogenous levels of total DDX19B protein
  • Spectrins are a family of filamentous cytoskeletal proteins that function as essential scaffold proteins that stabilize the plasma membrane and organize intracellular organelles
  • Spectrins are composed of alpha and beta dimers that associate to form tetramers linked in a head-to-head arrangement
  • This gene encodes an alpha spectrin that is specifically expressed in nonerythrocytic cells
  • The encoded protein has been implicated in other cellular functions including DNA repair and cell cycle regulation
  • Mutations in this gene are the cause of early infantile epileptic encephalopathy-5
  • Alternate splicing results in multiple transcript variants.