PIPA575976

Aladin Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA575976-Each-of-1 In Stock ₹ 46,502.50

PIPA575976 - 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

Aladin

Classification

Polyclonal

Conjugate

Unconjugated

Gene

AAAS

Gene Alias

AAA; Aaas; AAASb; achalasia, adrenocortical insufficiency, alacrimia; achalasia, adrenocortical insufficiency, alacrimia (Allgrove, triple-A); ADRACALA; Adracalin; ALADIN; aladin WD repeat nucleoporin; Allgrove, triple-A; D030041N15Rik; GL003

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

223921, 300259, 8086

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Form

Liquid

Applications

Western Blot

Concentration

1 mg/mL

Formulation

PBS with 50% glycerol and 0.02% sodium azide; pH 7.2

Gene Accession No.

P58742, Q9NRG9

Gene Symbols

AAAS

Immunogen

Synthetic peptide corresponding to amino acids 392-436 of Human Aladin.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

Related Products

Img

Thermo Scientific

PIPA554564

--

Img

Thermo Scientific

PIPA551572

--

Img

Novus Biologicals

NBP271358V

--

Img

Thermo Scientific

PIPA587206

--

Img

Thermo Scientific

PIPA561793

--

Img

Thermo Scientific

PIPA564315

--

Img

Thermo Scientific

PIPA561677

--

Img

Thermo Scientific

PIPA554399

--

Description

  • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 96% (by SDS-PAGE)
  • The protein encoded by this gene is a member of the WD-repeat family of regulatory proteins and may be involved in normal development of the peripheral and central nervous system
  • The encoded protein is part of the nuclear pore complex and is anchored there by NDC1
  • Defects in this gene are a cause of achalasia-addisonianism-alacrima syndrome (AAAS), also called triple-A syndrome or Allgrove syndrome
  • Two transcript variants encoding different isoforms have been found for this gene.