Recombinant Human Integrin alpha 6 beta 1 Protein, CF

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Product Details

Summary
Reactivity HuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

Order Details

Recombinant Human Integrin alpha 6 beta 1 Protein, CF Summary

Details of Functionality
Measured by its binding ability in a functional ELISA. When Recombinant Human Laminin alpha 4 (Catalog # 7340-A4) is coated at 5 μg/mL, Recombinant Human Integrin  alpha 6 beta 1 binds with apparent KD <2nM.
Source
Chinese Hamster Ovary cell line, CHO-derived human Integrin alpha 6 beta 1 protein
Human Integrin alpha 6
(Phe24-Ser1012)
Accession # NP_000201
GGGSGGGS Acidic Tail HHHHHH
Human Integrin beta 1
(Gln21-Asp728)
Accession # P05556
GGGSGGGS Basic Tail
N-terminus C-terminus
Accession #
N-terminal Sequence
Phe24 ( alpha 6 subunit) & Gln21 predicted: No results obtained, sequencing might be blocked ( beta 1 subunit)
Structure / Form
Noncovalently-linked heterodimer
Protein/Peptide Type
Recombinant Proteins
Purity
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain.
Endotoxin Note
<0.10 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
119 kDa ( alpha 6 subunit) & 86.4 kDa ( beta 1 subunit).
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
110-140 kDa & 140 - 170 kDa, reducing conditions
Publications
Read Publications using
7809-A6 in the following applications:

Packaging, Storage & Formulations

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.
  • 3 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS.
Purity
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain.
Reconstitution Instructions
Reconstitute at 400 μg/mL in PBS.

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Human Integrin alpha 6 beta 1 Protein, CF

  • CD49f
  • Integrin alpha 6 beta 1
  • ITGA6B
  • VLA-6

Background

Integrin alpha 6 beta 1, also called platelet glycoprotein GPIc-IIa, is a laminin binding integrin that is expressed on T cells, monocytes, endothelial cells, stem cells, and platelets (1-9). The non-covalent heterodimer is composed of ~150 kDa alpha 6/CD49f and 130 kDa beta 1/CD29 type I transmembrane glycoprotein subunits (2). While alpha 6 pairs only with beta 1 or beta 4, twelve integrins share the beta 1 subunit (1-5). The alpha 6 subunit is cleaved into extracellular heavy and transmembrane light chains (3). Alternative splicing in the human alpha 6 extracellular domain (ECD) at amino acid (aa) 216 creates X1 (ubiquitous), X2 and X1X2 isoforms, while splicing at a mouse or human cytoplasmic site creates A and B isoforms (10, 11). These forms do not appear to alter the binding specificity (4, 10, 11). The beta 1 ECD contains a vWFA domain, which participates in binding. Each subunit then has a transmembrane sequence and a short cytoplasmic tail. The dimer is folded when it is least active. Divalent cations and intracellular (inside-out) signaling convert it to its most active, extended and open conformation (1, 2). The human alpha 6 (X1) heavy chain shares 94‑95% aa identity with mouse, rat, bovine, and canine alpha 6, and the human beta 1 ECD shares 92‑96% aa sequence identity with rat, bovine, mouse, and feline beta 1. alpha 6 beta 1 shows broad specificity for adhesion to laminin isoforms (4, 10). Its expression on human and mouse pluripotent stem cells is important for attachment, expansion, and self‑renewal on LN‑511 (laminin  alpha 5  beta 1 gamma 1) (6, 7). The secreted protein Netrin-4 and the laminin  gamma 1 subunit form an adhesion‑activating complex with alpha 6 beta 1 on mouse neural stem cells and human lymphatic endothelial cells that promotes lymphangiogenesis (8, 9). alpha 6 beta 1 up‑regulation on cancers such as prostate, glioma, and hepatoma is reported to enhance tumorigenicity, motility, invasion and metastasis (12‑14). alpha 6 beta 1 cleavage via uPA (urokinase-type plasminogen activator) facilitates tumorigenicity in prostate cancers, and interaction of hepatoma alpha 6 beta 1 with EMMPRIN/CD147 may also enhance tumorigenicity by inducing uPA and other metalloproteinases (12, 13).
  1. Takada, Y. et al. (2007) Genome Biol. 8:215.
  2. Luo, B-H. et al. (2007) Annu. Rev. Immunol. 25:619.
  3. Tamura, R.N. et al. (1990) J. Cell Biol. 111:1593.
  4. Nishiuchi, R. et al. (2006) Matrix Biol. 25:189.
  5. Sonnenberg, A. and C.J.T. Linders (1990) J. Cell Science 96:207.
  6. Rodin, S. et al. (2010) Nat. Biotech. 28:611.
  7. Domogatskaya A. et al. (2008) Stem Cells 26:2800.
  8. Staquicini, F.I. et al. (2009) Proc. Natl. Acad. Sci. USA 106:2903.
  9. Larrieu-Lahargue, F. et al. (2011) Circ. Res. 109:770.
  10. Delwel, G. O. et al. (1995) Cell Adhes. Commun. 3:143.
  11. Hogervorst, F. et al. (1993) J. Cell Biol. 121:179.
  12. Sroka, I.C. et al. (2011) Mol. Cancer Res. 9:1319.
  13. Dai, J.Y. et al. (2009) BMC Cancer 9:337.
  14. Delamarre, E. et al. (2009) Am. J. Pathol. 175:844.

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