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Antibody used in IHC on Human Heart.
Antibody used in IHC on Human Liver.
Antibody used in WB on Transfected 293T at 1.25 ug/ml.
Antibody used in IHC on Human Heart.

DLX5 Antibody

CATALOG NUMBER: 28-898

Clonality:
Polyclonal
Tested Applications:
ELISA, IHC, WB
Host Species:
Rabbit
Species Reactivity:
Dog, Human, Mouse, Rat
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Dog, Human, Mouse, Rat
Immunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human DLX5.
Conjugate:
Unconjugated
Tested Applications:
ELISA, IHC, WB
Application Note:
DLX5 antibody can be used for detection of DLX5 by ELISA at 1:1562500. DLX5 antibody can be used for detection of DLX5 by western blot at 1.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Positive Control 1:
Tranfected 293T Cell Lysate
Predicted Molecular Weight:
31 kDa
Purification:
Antibody is purified by protein A chromatography method.
Clonality:
Polyclonal
Physical State:
Liquid
Buffer:
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration:
batch dependent
Storage Conditions:
For short periods of storage (days) store at 4°C. For longer periods of storage, store DLX5 antibody at -20°C. As with any antibody avoid repeat freeze-thaw cycles.
Ncbi Official Symbol:
DLX5
Additional Names:
DLX5, SHFM1D
Protein Accession Number:
NP_005212
Protein Gi Number:
4885187
Ncbi Gene Id Number:
1749
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
DLX5 is a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. This protein may play a role in bone development and fracture healing. Mutation in its gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation.This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation.
Background Reference 1:
van (2006) Calcif. Tissue Int. 78 (2), 98-102.

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
This product is for research use only.

CATALOG NUMBER:

28-898

List Size:
100 ul

List Price:

$473.00

Datasheet
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