Human Semaphorin 6A Antibody

Catalog # Availability Size / Price Qty
AF1146
AF1146-SP
Product Details
Citations (5)
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Human Semaphorin 6A Antibody Summary

Species Reactivity
Human
Specificity
Detects human Semaphorin 6A in direct ELISAs and Western blots. In direct ELISAs, approximately 40% cross-reactivity with recombinant mouse Semaphorin 6A is observed.
Source
Polyclonal Goat IgG
Purification
Antigen Affinity-purified
Immunogen
Mouse myeloma cell line NS0-derived recombinant human Semaphorin 6A
Gly19-Thr649
Accession # Q9H2E6
Formulation
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.
Label
Unconjugated

Applications

Recommended Concentration
Sample
Western Blot
0.1 µg/mL
Recombinant Human Semaphorin 6A Fc Chimera (Catalog # 1146-S6)
Flow Cytometry
2.5 µg/106 cells
Human T cells treated with PHA
Immunohistochemistry
5-15 µg/mL
Immersion fixed paraffin-embedded sections of human spinal cord
CyTOF-ready
Ready to be labeled using established conjugation methods. No BSA or other carrier proteins that could interfere with conjugation.
 

Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.

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Preparation and Storage

Reconstitution
Reconstitute at 0.2 mg/mL in sterile PBS.
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Shipping
Lyophilized product is shipped at ambient temperature. Liquid small pack size (-SP) is shipped with polar packs. Upon receipt, store immediately at the temperature recommended below.
Stability & Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 6 months, -20 to -70 °C under sterile conditions after reconstitution.

Background: Semaphorin 6A

The semaphorins constitute a large family of secreted, glycosylphosphatidylinositol (GPI)-anchored and transmembrane cell signaling molecules. Depending on their domain organization and species origin, these proteins can be classified into eight groups. To date, at least 19 vertebrate Semaphorins belonging to five groups (class 3 to 7), have been identified. All Semaphorins contain a conserved 500 amino acid (aa) Sema domain at the amino-terminus. Semaphorins are best known for their roles in axon guidance during neuronal development. They are also expressed in non-neuronal tissues and are involved in angiogenesis, hematopoiesis, organogenesis, and the regulation of immune functions (1, 2). Class 6 Semaphorins (Sema 6) are transmembrane proteins that share homology with the axon-guiding insect Sema 1A. Human Sema 6A (VIa) cDNA predicts a 1,030 aa protein comprised of an extracellular domain, a transmembrane domain, and a long cytoplasmic tail (3, 4). A secreted form of Sema 6A can repel sympathetic and dorsal root ganglion axons in vitro, indicating a traditional role as an axon guidance signal (5). There is evidence, however, that Sema 6A also functions as a guidance receptor. Sema 6A mutants show a defect in thalamocortical neuron projection that is cell autonomous, and the cytoplasmic tails for Sema 6 contain binding sites for intracellular regulatory molecules such as Evl and Src (6).

References
  1. Fiore, R. and A.W. Puschel (2003) Frontiers Biosci. 8:484.
  2. Goshima, Y. et al. (2002) J. Clin. Invest. 109:993.
  3. Zhou, et al. (1997) Mol. Cell Neurosci. 9:26.
  4. Kikuchi, K. et al. (1999) Mol. Cell Neurosci. 13:9.
  5. Xu, X-M. et al. (2000) J. Neurosci. 20:2638.
  6. Leighton, P.A. et al. (2001) Nature 410:174.
Entrez Gene IDs
57556 (Human); 20358 (Mouse)
Alternate Names
KIAA1368HT018; sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A; Sema VIA; SEMA; Sema6A; SEMA6A1; SEMA6A-1; Semaphorin 6A; semaphorin 6A-1; Semaphorin VIA; semaphorin-6A; semaphorin-6A-1; SEMAQ; VIA

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Citations for Human Semaphorin 6A Antibody

R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.

5 Citations: Showing 1 - 5
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  1. miR-27a regulates vascular remodeling by targeting endothelial cells' apoptosis and interaction with vascular smooth muscle cells in aortic dissection
    Authors: Y Sun, Y Xiao, H Sun, Z Zhao, J Zhu, L Zhang, J Dong, T Han, Q Jing, J Zhou, Z Jing
    Theranostics, 2019-10-18;9(25):7961-7975.
    Species: Human
    Sample Types: Cell Lysates
    Applications: Western Blot
  2. Shear stress-regulated miR-27b controls pericyte recruitment by repressing SEMA6A and SEMA6D
    Authors: S Demolli, A Doddaballa, K Devraj, K Stark, Y Manavski, A Eckart, CM Zehendner, T Lucas, T Korff, M Hecker, S Massberg, S Liebner, D Kaluza, RA Boon, S Dimmeler
    Cardiovasc. Res., 2017-05-01;113(6):681-691.
    Species: Human
    Sample Types: Cell Lysates
    Applications: Western Blot
  3. MicroRNA-27a/b controls endothelial cell repulsion and angiogenesis by targeting semaphorin 6A.
    Authors: Urbich C, Kaluza D, Fromel T, Knau A, Bennewitz K, Boon RA, Bonauer A, Doebele C, Boeckel JN, Hergenreider E, Zeiher AM, Kroll J, Fleming I, Dimmeler S
    Blood, 2011-12-19;119(6):1607-16.
    Species: Human
    Sample Types: Cell Lysates
    Applications: Western Blot
  4. A meta-analysis of human embryonic stem cells transcriptome integrated into a web-based expression atlas.
    Authors: Assou S, Le Carrour T, Tondeur S, Strom S, Gabelle A, Marty S, Nadal L, Pantesco V, Reme T, Hugnot JP, Gasca S, Hovatta O, Hamamah S, Klein B, De Vos J
    Stem Cells, 2007-01-04;25(4):961-73.
    Species: Human
    Sample Types: Whole Cells
    Applications: ICC
  5. Myogenesis modelled by human pluripotent stem cells: a multi‐omic study of Duchenne myopathy early onset
    Authors: Virginie Mournetas, Emmanuelle Massouridès, Jean‐Baptiste Dupont, Etienne Kornobis, Hélène Polvèche, Margot Jarrige et al.
    Journal of Cachexia, Sarcopenia and Muscle

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