DCX Polyclonal Antibody

Elabscience
Product Code: E-AB-19408
Product Group: Primary Antibodies
Supplier: Elabscience
CodeSizePrice
E-AB-19408-20uL20uL£125.00
Quantity:
E-AB-19408-60uL60uL£172.00
Quantity:
E-AB-19408-120uL120uL£237.00
Quantity:
E-AB-19408-200uL200uL£344.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Host Type: Rabbit
Antibody Isotype: IgG
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Target Species: Human
Applications:
  • Enzyme-Linked Immunosorbent Assay (ELISA)
  • Immunohistochemistry (IHC)
  • Western Blot (WB)
Shipping:
Ice packs
Storage:
Store at -20°C. Avoid freeze / thaw cycles.

Images

1 / 2
Immunohistochemistry of paraffin-embedded Human tonsil tissue  using DCX Polyclonal Antibody at dilution of 1:35(?200)
2 / 2
Immunohistochemistry of paraffin-embedded Human colorectal cancer tissue  using DCX Polyclonal Antibody at dilution of 1:35(?200)

Immunohistochemistry of paraffin-embedded Human tonsil tissue  using DCX Polyclonal Antibody at dilution of 1:35(?200)
Immunohistochemistry of paraffin-embedded Human colorectal cancer tissue  using DCX Polyclonal Antibody at dilution of 1:35(?200)

Documents

Further Information

Abbreviation:
DCX
Background:
This gene encodes a member of the doublecortin family. The protein encoded by this gene is a cytoplasmic protein and contains two doublecortin domains, which bind microtubules. In the developing cortex, cortical neurons must migrate over long distances to reach the site of their final differentiation. The encoded protein appears to direct neuronal migration by regulating the organization and stability of microtubules. In addition, the encoded 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 this gene cause abnormal migration of neurons during development and disrupt the layering of the cortex, leading to epilepsy, cognitive disability, subcortical band heterotopia ("double cortex" syndrome) in females and lissencephaly ("smooth brain" syndrome) in males. Multiple transcript variants encoding different isoforms have been found for this gene.
Buffer:
PBS with 0.05% NaN3 and 40% Glycerol,pH7.4
Calculated MW:
49 kDa
Concentration:
1.3 mg/mL
Conjugation:
Unconjugated
Dilution:
WB 1:500-1:2000, IHC 1:25-1:100, ELISA 1:5000-1:10000
Immunogen:
Synthetic peptide of human DCX
ObservedMW:
Refer to figures
Purification method:
Antigen affinity purification
Target Synonym:
DBCN;Dbct;DC;DCX;DCX;Doublecortex;Doublin;FLJ51296;Lis X;Lis-X;Lissencephalin X;Lissencephalin-X;Lissencephaly X linked;Lissencephaly X linked doublecortin;LISX;Neuronal migration protein doublecortin;OTTHUMP00000023859;OTTHUMP00000023860;OTTHUMP00000216315;OTTHUMP00000216316;SCLH;XLIS
UNIProt ID:
O43602