Recombinant human Ephrin B1 protein (ab181909)
Key features and details
- Expression system: HEK 293 cells
- Purity: > 95% SDS-PAGE
- Endotoxin level: < 1.000 Eu/µg
- Active: Yes
- Tags: His tag C-Terminus
- Suitable for: SDS-PAGE, Functional Studies
Description
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Product name
Recombinant human Ephrin B1 protein
See all Ephrin B1 proteins and peptides -
Biological activity
Measured by its binding ability in a functional ELISA.
Immobilised ab181909 at 10 µg/ml can bind Human EPHB6 with a linear range of 0.2-8 µg/ml.
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Purity
> 95 % SDS-PAGE. -
Endotoxin level
< 1.000 Eu/µg -
Expression system
HEK 293 cells -
Accession
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Protein length
Protein fragment -
Animal free
No -
Nature
Recombinant -
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Species
Human -
Sequence
LAKNLEPVSWSSLNPKFLSGKGLVIYPKIGDKLDIICPRAEAGRPYEYYK LYLVRPEQAAACSTVLDPNVLVTCNRPEQEIRFTIKFQEFSPNYMGLEFK KHHDYYITSTSNGSLEGLENREGGVCRTRTMKIIMKVGQDPNAVTPEQLT TSRPSKEADNTVKMATQAPGSRGSLGDSDGKHETVNQEEKSGPGASGGSS GDPDG -
Predicted molecular weight
23 kDa including tags -
Amino acids
28 to 232 -
Tags
His tag C-Terminus -
Additional sequence information
NP_004420
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Associated products
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Related Products
Specifications
Our Abpromise guarantee covers the use of ab181909 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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Applications
SDS-PAGE
Functional Studies
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Form
Lyophilized -
Concentration information loading...
Preparation and Storage
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Stability and Storage
Shipped at 4°C. Store at 4°C prior to reconstitution. Store at -80°C. Avoid freeze / thaw cycle. For long term storage it is recommended to add a carrier protein on reconstitution (0.1% HSA or BSA).
pH: 7.40
Constituents: 95% PBS, 5% TrehaloseThis product is an active protein and may elicit a biological response in vivo, handle with caution.
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ReconstitutionReconstitute with sterile deionized water to a concentration of 300 µg/ml.
General Info
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Alternative names
- CFND
- CFNS
- Craniofrontonasal syndrome (craniofrontonasal dysplasia)
see all -
Function
Binds to the receptor tyrosine kinases EPHB1 and EPHA1. Binds to, and induce the collapse of, commissural axons/growth cones in vitro. May play a role in constraining the orientation of longitudinally projecting axons. -
Tissue specificity
Heart, placenta, lung, liver, skeletal muscle, kidney, pancreas. -
Involvement in disease
Defects in EFNB1 are a cause of craniofrontonasal syndrome (CFNS) [MIM:304110]; also known as craniofrontonasal dysplasia (CFND). CFNS is an X-linked inherited syndrome characterized by hypertelorism, coronal synostosis with brachycephaly, downslanting palpebral fissures, clefting of the nasal tip, joint anomalies, longitudinally grooved fingernails and other digital anomalies. -
Sequence similarities
Belongs to the ephrin family. -
Post-translational
modificationsInducible phosphorylation of tyrosine residues in the cytoplasmic domain. -
Cellular localization
Membrane. - Information by UniProt
Images
Protocols
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
Datasheets and documents
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Datasheet download
References (0)
ab181909 has not yet been referenced specifically in any publications.