HOXD10 Antibody - middle region : FITC

Referencia P100936_P050-FITC

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HOXD10 Antibody - middle region (P100936_P050)

Datasheets/ManualsPrintable datasheet for anti-HOXD10 (P100936_P050) antibody
Product Info
Tested Species ReactivityHuman
Predicted Species ReactivityMouse, Rat, Cow, Dog, Horse, Pig, Rabbit
Product FormatLiquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
ClonalityPolyclonal
HostRabbit
ApplicationWB
Reconstitution and StorageFor short term use, store at 2-8C up to 1 week. For long term storage, store at -20C in small aliquots to prevent freeze-thaw cycles.
ImmunogenThe immunogen is a synthetic peptide directed towards the middle region of human HOXD10
PurificationAffinity Purified
Predicted Homology Based on Immunogen SequenceCow: 100%; Dog: 100%; Horse: 100%; Mouse: 100%; Pig: 100%; Rabbit: 100%; Rat: 92%
Peptide SequenceSynthetic peptide located within the following region: NPEVPVPGYFRLSQTYATGKTQEYNNSPEGSSTVMLQLNPRGAAKPQLSA
Concentration0.5 mg/ml
Blocking PeptideFor anti-HOXD10 (P100936_P050) antibody is Catalog # AAP31289 (Previous Catalog # AAPP02038)
ReferenceGurnett,C.A., Clin. Orthop. Relat. Res. 462, 27-31 (2007)
Gene SymbolHOXD10
Gene Full NameHomeobox D10
Alias SymbolsHOX4, HOX4D, HOX4E, Hox-4.4
NCBI Gene Id3236
Protein NameHomeobox protein Hox-D10
Description of TargetHOXD10 is the sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis.This gene is a member of the Abd-B homeobox family and encodes a protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox D genes located on chromosome 2. The encoded nuclear protein functions as a sequence-specific transcription factor that is expressed in the developing limb buds and is involved in differentiation and limb development. Mutations in this gene have been associated with Wilm's tumor and congenital vertical talus (also known as 'rocker-bottom foot' deformity or congenital convex pes valgus) and/or a foot deformity resembling that seen in Charcot-Marie-Tooth disease. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Uniprot IDP28358
Protein Accession #NP_002139
Nucleotide Accession #NM_002148
Protein Size (# AA)340
Molecular Weight38kDa
Protein InteractionsEP300; CREBBP; PBX1; GMNN; HMGB1;