HoxA11/D11 rabbit pAb

HoxA11/D11 rabbit pAb

AO-06-ES2556-100

HoxA11/D11 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES2556
Product nameHoxA11/D11 rabbit pAb
ReactivityHuman;Mouse
ApplicationsWB;IHC;IF;ELISA
Other nameHOXA11; HOX1I; Homeobox protein Hox-A11; Homeobox protein Hox-1I; HOXD11; HOX4F; Homeobox protein Hox-D11; Homeobox protein Hox-4F
Size100μL
Unit price ($)248
Human gene ID3207/3237
Human Swiss-ProtP31270/P31277
SourceRabbit
IsotypeIgG
TargetHoxA11/D11
Fields>>Transcriptional misregulation in cancer
Gene nameHOXA11/HOXD11
Protein nameHomeobox protein Hox-A11/D11
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID15396/15431
Mouse gene linkView Mouse Gene
Mouse Swiss-Prot
Mouse Swiss link
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from human HOXA11/D11. AA range:216-265
SpecificityHoxA11/D11 Polyclonal Antibody detects endogenous levels of HoxA11/D11 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/20000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)28kD
BackgroundIn vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is involved in the regulation of uterine development and is required for female fertility. Mutations in this gene can cause radio-ulnar synostosis with amegakaryocytic thrombocytopenia. [provided by RefSeq, Jul 2008],
Functiondisease:Defects in HOXA11 are the cause of radioulnar synostosis with amegakaryocytic thrombocytopenia [MIM:605432]. The syndrome consists of an unusual association of bone marrow failure and skeletal defects. Patients have the same skeletal defects, the proximal fusion of the radius and ulna, resulting in extremely limited pronation and supination of the forearm. Some patients have also symptomatic thrombocytopenia, with bruising and bleeding problems since birth, necessitating correction by bone marrow or umbilical-cord stem-cell transplantation.,function:Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis.,similarity:Belongs to the Abd-B homeobox family.,similarity:Contains 1 homeobox DNA-binding domain.,
Subcellular locationNucleus.
ExpressionOvary,

Additional Images

Image 1
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Western Blot analysis of various cells using HoxA11/D11 Polyclonal Antibody diluted at 1:500 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit (SC-003,Inventbiotech,MN,USA).
Image 2
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Western Blot analysis of 293T-UV cells using HoxA11/D11 Polyclonal Antibody diluted at 1:500 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit (SC-003,Inventbiotech,MN,USA).
Image 3
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Immunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.
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Immunofluorescence analysis of HUVEC cells, using HOXA11/D11 Antibody. The picture on the right is blocked with the synthesized peptide.
: AO-06-ES2556-100
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