PIPA5102854

Phospho-Doublecortin (Ser335) Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5102854-Each-of-1 In Stock ₹ 41,607.50

PIPA5102854 - Each of 1

₹ 41,607.50

In Stock

Quantity

1

Base Price: ₹ 41,607.50

GST (18%): ₹ 7,489.35

Total Price: ₹ 49,096.85

Antigen

Phospho-Doublecortin (Ser335)

Classification

Polyclonal

Conjugate

Unconjugated

Gene

DCX

Gene Alias

DBCN; Dbct; DC; Dcn; DCX; doublecortex; doublecortin; doublin; lissencephalin-X; lissencephaly, X-linked (doublecortin); LISX; Lis-X; LIS-XD; Neuronal migration protein doublecortin; OTTHUMP00000023860; OTTHUMP00000216316; SCLH; XLIS

Host Species

Rabbit

Purification Method

sequential chromatography

Regulatory Status

RUO

Gene ID (Entrez)

13193, 1641, 84394

Content And Storage

-20°C

Form

Liquid

Applications

Immunohistochemistry (Paraffin), Western Blot

Concentration

1 mg/mL

Formulation

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

Gene Accession No.

O43602, O88809, Q9ESI7

Gene Symbols

DCX

Immunogen

A synthesized peptide derived from human DCX(Accession O43602), corresponding to amino acid residues around phosphorylated Ser335.

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 Doublecortin only when phosphorylated at Ser335
  • In the developing cortex, cortical neurons must migrate over long distances to reach the site of their final differentiation
  • DCX is a cytoplasmic protein which appears to direct neuronal migration by regulating the organization and stability of microtubules
  • It contains two doublecortin domains, which bind microtubules
  • In addition, this protein interacts with LIS1, the regulatory gamma subunit of platelet activating factor acetylhydrolase, and this interaction is important to proper microtubule function in the developing cortex
  • Mutations in the gene encoding DCX are a cause of X-linked lissencephaly.