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ABE1402

Sigma-Aldrich

Anti-LHX2 Antibody

serum, from rabbit

Sinónimos:

LIM/homeobox protein Lhx2, Homeobox protein LH-2, LIM homeobox protein, LHX2

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About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.43

biological source

rabbit

Quality Level

antibody form

serum

antibody product type

primary antibodies

clone

polyclonal

species reactivity

mouse, human

technique(s)

ChIP: suitable (ChIP-seq)
immunofluorescence: suitable
western blot: suitable

NCBI accession no.

UniProt accession no.

shipped in

dry ice

target post-translational modification

unmodified

Gene Information

mouse ... Lhx2(16870)

General description

LIM/homeobox protein Lhx2 (UniProt Q9Z0S2; also known as Homeobox protein LH-2, LIM homeo box protein 2, Lim2) is encoded by the Lhx2 gene (Gene ID 16870) in murine species. Lhx2 is a transcription factor that plays an important role in controlling the behavior of progenitor cells involved in the development of the skin hair cycling, eye, forebrain, limb, hematopoietic, olfactory, and pituitary systems. Lhx2 is shown to regulate a significant number of hair follicle stem cell (HF-SC) signature genes, as well as cytoskeletal and adhesion molecules within the niche where HF-SCs reside as a single layer of polarized, quiescent epithelial cells. Lhx2 deficiency leads to baldness, because the niche can no longer anchor its hair and maintain the proper behavior of its SCs as a result of greatly perturbed HF-SCs polarization and niche architecture.

Immunogen

Recombinant protein corresponding to mouse LHX2.

Application

Immunofluorescence Analysis: A representative lot detected Lhx2 immunoreactivity by fluorescent immunohistochemistry using OCT-embedded, PFA-fixed backskin cryosections from wild-type, but not Lhx2 knockout, mice at varies developmental stages, including E16.5, P0, P30, and the second telogen (Folgueras, A.R., et. al. (2013). Cell Stem Cell. 13(3):314-327).
Chromatin Immunoprecipitation Analysis: A representative lot detected Lhx2-targeted promoter and enhancer regions using α6hi/CD34+ skin cells enriched in hair follicle stem cells (HF-SCs) from mice at the second telogen developmental stage (Folgueras, A.R., et. al. (2013). Cell Stem Cell. 13(3):314-327).
Chromatin Immunoprecipitation-Sequencing Analysis: A representative lot detected Lhx2-targeted promoter and enhancer regions by a genome-wide ChIP-seq analysis using α6hi/CD34+ skin cells enriched in hair follicle stem cells (HF-SCs) from mice at the second telogen developmental stage (Folgueras, A.R., et. al. (2013). Cell Stem Cell. 13(3):314-327).
Immunofluorescence Analysis: A representative lot (1:1,000 dilution) detected Lhx2 immunoreactivity in human skin samples by fluorescent immunohistochemistry using OCT-embedded, PFA-fixed cryosections (Data courtesy of Dr. Elaine Fuchs, Howard Hughes Medical Institute, The Rockefeller University ).
Research Category
Epigenetics & Nuclear Function
Research Sub Category
Nuclear Receptors
This Anti-LHX2 Antibody is validated for use in Western Blotting, Immunofluorescence, ChIP-seq and Chromatin Immunoprecipitation (ChIP) for the detection of LHX2.

Quality

Evaluated by Western Blotting in Murine keratinocyte K14rtTA-LHX2-TRE cell lysate.

Western Blotting Analysis: A 1:5,000 dilution of this antibody detected doxycycline-induced LHX2 expression in 10 µg of Murine keratinocyte K14rtTA-LHX2-TRE cell lysate.

Target description

~48 kDa detected. Target band size appears larger than the calculated molecular weight of 44.4 kDa due to posttranslational glycosylation. Uncharacterized band(s) may appear in some lysates.

Physical form

Rabbit polyclonal serum with 0.05% sodium azide.
Unpurified

Storage and Stability

Stable for 1 year at -20°C from date of receipt.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.

Other Notes

Concentration: Please refer to lot specific datasheet.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Alina Stegemann et al.
Nature neuroscience, 26(5), 820-829 (2023-04-07)
A painful episode can lead to a life-long increase in an individual's experience of pain. Fearful anticipation of imminent pain could play a role in this phenomenon, but the neurobiological underpinnings are unclear because fear can both suppress and enhance
Anna Welle et al.
Glia, 69(9), 2160-2177 (2021-05-25)
Astrocytes from the cerebral cortex (CTX) and cerebellum (CB) share basic molecular programs, but also form distinct spatial and functional subtypes. The regulatory epigenetic layers controlling such regional diversity have not been comprehensively investigated so far. Here, we present an
Varun Suresh et al.
PLoS genetics, 19(8), e1010874-e1010874 (2023-08-18)
In the mammalian cerebral cortex, the hippocampal primordium (Hcp) occupies a discrete position in the dorsal telencephalic neuroepithelium adjacent to the neocortical primordium (Ncp). We examined transcriptomic and chromatin-level features that distinguish the Hcp from the Ncp in the mouse
Bianca M Lupan et al.
Development (Cambridge, England), 150(10) (2023-05-04)
Mutations in components of the exon junction complex (EJC) are associated with neurodevelopment and disease. In particular, reduced levels of the RNA helicase EIF4A3 cause Richieri-Costa-Pereira syndrome (RCPS) and copy number variations are linked to intellectual disability. Consistent with this
Katherine S Matho et al.
Nature, 598(7879), 182-187 (2021-10-08)
Diverse types of glutamatergic pyramidal neurons mediate the myriad processing streams and output channels of the cerebral cortex1,2, yet all derive from neural progenitors of the embryonic dorsal telencephalon3,4. Here we establish genetic strategies and tools for dissecting and fate-mapping

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