PIPA5103193

TPX2 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5103193-Each-of-1 In Stock ₹ 46,502.50

PIPA5103193 - 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

TPX2

Classification

Polyclonal

Conjugate

Unconjugated

Gene

Tpx2

Gene Alias

2610005B21Rik; C20orf1; C20orf2; Differentially expressed in cancerous and non-cancerous lung cells 2; differentially expressed in lung cells; DIL2; DIL-2; FLS353; GD: HCA519; GD:C20orf1; HCA519; HCTP4; Hepatocellular carcinoma-associated antigen 519; hepatocellular carcinoma-associated antigen 90; p100; preferentially expressed in colorectal cancer; protein fls353; REPP86; restricted expression proliferation associated protein 100; restricted expression proliferation-associated protein 100; Targeting protein for Xklp2; TPX 2; Tpx2; TPX2 microtubule nucleation factor; TPX2, microtubule nucleation factor; TPX2, microtubule-associated; TPX2, microtubule-associated protein homolog; TPX2, microtubule-associated protein homolog (Xenopus laevis); TPX2, microtubule-associated, homolog

Host Species

Rabbit

Purification Method

Affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

22974, 311546, 72119

Content And Storage

-20°C

Form

Liquid

Applications

Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot

Concentration

1 mg/mL

Formulation

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

Gene Accession No.

A2APB8, Q9ULW0

Gene Symbols

Tpx2

Immunogen

A synthesized peptide derived from human TPX2(Accession Q9ULW0), corresponding to amino acid residues K685-V735.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

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Description

  • Antibody detects endogenous levels of total DIL-2
  • The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome
  • This gene is intronless
  • Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT).