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anti-Short Stature Homeobox (SHOX) Antibodies

SHOX belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Additionally we are shipping SHOX Proteins (2) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
SHOX 6473 O15266
SHOX    
SHOX    
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Top anti-SHOX Antibodies at antibodies-online.com

Showing 10 out of 25 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Chicken Rabbit Un-conjugated WB 100 μL Log in to see 2 to 3 Days
$289.00
Details
Human Rabbit Un-conjugated WB 50 μg Log in to see 8 to 10 Days
$551.83
Details
Chicken Rabbit Un-conjugated WB Western blot analysis of SHOX expression in HEK293T (A), Raw264.7 (B), SP2/0 (C) whole cell lysates. 200 μL Log in to see 9 Days
$487.50
Details
Human Rabbit Un-conjugated ELISA, WB 50 μg Log in to see 2 to 3 Days
$433.13
Details
Human Rabbit FITC ELISA, WB   200 μL Log in to see 8 to 10 Days
$969.83
Details
Human Rabbit Un-conjugated WB   100 μL Log in to see 8 to 10 Days
$375.83
Details
Human Rabbit Un-conjugated ELISA   200 μL Log in to see 8 to 10 Days
$713.17
Details
Human Mouse Un-conjugated WB Western Blot analysis of SHOX expression in transfected 293T cell line by SHOX MaxPab polyclonal antibody.Lane 1: SHOX transfected lysate(24.75 KDa).Lane 2: Non-transfected lysate. SHOX MaxPab polyclonal antibody. Western Blot analysis of SHOX expression in human liver. 50 μg Log in to see 9 Days
$430.00
Details
Human Rabbit Un-conjugated ELISA, WB   200 μL Log in to see 11 to 16 Days
$531.14
Details
Human Rabbit Un-conjugated WB   100 μL Log in to see 8 to 10 Days
$581.17
Details

SHOX Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality Conjugate
Human ,
,

, , , , ,
Mouse (Murine)


Chicken


Top referenced anti-SHOX Antibodies

  1. Chicken Polyclonal SHOX Primary Antibody for WB - ABIN2777838 : Messina, Aguennouz, Arrigo, Rodolico, Valenzise, Musumeci, Vita, Lanzano, De Luca: Novel SHOX gene mutation in a short boy with Becker muscular dystrophy: double trouble in two adjacent genes. in Hormone research 2008 (PubMed)

More Antibodies against SHOX Interaction Partners

Zebrafish Short Stature Homeobox (SHOX) interaction partners

  1. demonstrate evolutionarily conserved Shox plays roles in early embryonic growth and in later bone formation.

  2. The expression pattern of the shox gene across the whole embryo and characterise the enhancer domains of different conserved non-coding elements associated with this gene, is reported.

Human Short Stature Homeobox (SHOX) interaction partners

  1. SHOX haploinsufficiency is associated with 45,X disorder of sexual differentiation.

  2. Microduplications involving SHOX cause Idiopathic short stature by disrupting the cis (show CISH Antibodies)-regulatory machinery of this gene.

  3. Mutation analysis of the SHOX gene indicated that a novel heterozygous deletion mutation of SHOX was responsible for the isolated Madelung deformity disease

  4. mutations in SHOX gene may have an impact on bone microarchitecture albeit not bone strength

  5. Polymorphic variants detected in exon 1 of SHOX gene associated with idiopathic short stature.

  6. Findings support the hypothesis that SHOX may play a central role in the regulation of the cell death pathways activated during long bone development.

  7. report the autoptic, histological and radiographic phenotype of two fetuses (22 and 12 weeks) with Langer mesomelic dysplasia, a homozygous deletion of the 3' enhancer of the SHOX gene, and consanguineous parents affected by Leri-Weill dyschondrosteosis

  8. Abnormal body proportions were observed in almost all individuals with SHOX-D, 50% of females with TS and 16% of children considered idiopathic short stature.

  9. Although human SHOX can exert similar functions to mouse Shox2 (show SHOX2 Antibodies) in regulating early temporomandibular joint development, it apparently has a distinct function in the regulation of those molecules that are involved in tissue homeostasis.

  10. Data provide new information about the spectrum of phenotypic alterations showed by Leri-Weill dyschondrosteosis patients with different deletions of the SHOX enhancer region.

SHOX Antigen Profile

Protein Summary

This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

Gene names and symbols associated with SHOX

  • short stature homeobox (shox) antibody
  • short stature homeobox (SHOX) antibody
  • GCFX antibody
  • PHOG antibody
  • SHOXY antibody
  • si:ch211-134k13.1 antibody
  • SS antibody
  • zgc:123182 antibody

Protein level used designations for SHOX

short stature homeobox protein , growth control factor, X-linked , pseudoautosomal homeobox-containing osteogenic protein

GENE ID SPECIES
664748 Danio rerio
418669 Gallus gallus
491706 Canis lupus familiaris
615159 Bos taurus
6473 Homo sapiens
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