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GALNT11 Protein (AA 30-608) (His tag)

Crystallography grade GALNT11 Origin: Human Host: Insect Cells Recombinant >95 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. ELISA, SDS, WB, Crys
Catalog No. ABIN3092802
  • Target See all GALNT11 products
    GALNT11 (UDP-N-Acetyl-alpha-D-Galactosamine:polypeptide N-Acetylgalactosaminyltransferase 11 (GalNAc-T11) (GALNT11))
    Protein Type
    Recombinant
    Protein Characteristics
    AA 30-608
    Origin
    • 2
    • 1
    Human
    Source
    • 3
    Insect Cells
    Purification tag / Conjugate
    This GALNT11 protein is labelled with His tag.
    Application
    ELISA, SDS-PAGE (SDS), Western Blotting (WB), Crystallization (Crys)
    Sequence
    FSEVTQPLKN VPVKGSGPHG PSPKKFYPRF TRGPSRVLEP QFKANKIDDV IDSRVEDPEE GHLKFSSELG MIFNERDQEL RDLGYQKHAF NMLISDRLGY HRDVPDTRNA ACKEKFYPPD LPAASVVICF YNEAFSALLR TVHSVIDRTP AHLLHEIILV DDDSDFDDLK GELDEYVQKY LPGKIKVIRN TKREGLIRGR MIGAAHATGE VLVFLDSHCE VNVMWLQPLL AAIREDRHTV VCPVIDIISA DTLAYSSSPV VRGGFNWGLH FKWDLVPLSE LGRAEGATAP IKSPTMAGGL FAMNRQYFHE LGQYDSGMDI WGGENLEISF RIWMCGGKLF IIPCSRVGHI FRKRRPYGSP EGQDTMTHNS LRLAHVWLDE YKEQYFSLRP DLKTKSYGNI SERVELRKKL GCKSFKWYLD NVYPEMQISG SHAKPQQPIF VNRGPKRPKV LQRGRLYHLQ TNKCLVAQGR PSQKGGLVVL KACDYSDPNQ IWIYNEEHEL VLNSLLCLDM SETRSSDPPR LMKCHGSGGS QQWTFGKNNR LYQVSVGQCL RAVDPLGQKG SVAMAICDGS SSQQWHLEG
    Sequence without tag. Tag location is at the discretion of the manufacturer. If you have a special request, please contact us.
    Characteristics
    • Made in Germany - from design to production - by highly experienced protein experts.
    • Human GALNT11 Protein (raised in Insect Cells) purified by multi-step, protein-specific process to ensure crystallization grade.
    • State-of-the-art algorithm used for plasmid design (Gene synthesis).

    This protein is a made to order protein and will be made for the first time for your order. Our experts in the lab will ensure that you receive a correctly folded protein.

    The big advantage of ordering our made-to-order proteins in comparison to ordering custom made proteins from other companies is that there is no financial obligation in case the protein cannot be expressed or purified.

    In the unlikely event that the protein cannot be expressed or purified we do not charge anything (other companies might charge you for any performed steps in the expression process for custom-made proteins, e.g. fees might apply for the expression plasmid, the first expression experiments or purification optimization).

    When you order this made-to-order protein you will only pay upon receival of the correctly folded protein. With no financial risk on your end you can rest assured that our experienced protein experts will do everything to make sure that you receive the protein you ordered.

    The concentration of our recombinant proteins is measured using the absorbance at 280nm. The protein's absorbance will be measured in several dilutions and is measured against its specific reference buffer.

    The concentration of the protein is calculated using its specific absorption coefficient. We use the Expasy's protparam tool to determine the absorption coefficient of each protein.

    Purification
    Two step purification of proteins expressed in baculovirus infected SF9 insect cells:
    1. In a first purification step, the protein is purified from the cleared cell lysate using three different His-tag capture materials: high yield, EDTA resistant, or DTT resistant. Eluate fractions are analyzed by SDS-PAGE.
    2. Protein containing fractions of the best purification are subjected to second purification step through size exclusion chromatography. Eluate fractions are analyzed by SDS-PAGE and Western blot.
    Purity
    >95 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot.
    Sterility
    0.22 μm filtered
    Endotoxin Level
    Protein is endotoxin free.
    Grade
    Crystallography grade
  • Application Notes
    In addition to the applications listed above we expect the protein to work for functional studies as well. As the protein has not been tested for functional studies yet we cannot offer a gurantee though.
    Comment

    In cases in which it is highly likely that the recombinant protein with the default tag will be insoluble our protein lab may suggest a higher molecular weight tag (e.g. GST-tag) instead to increase solubility. We will discuss all possible options with you in detail to assure that you receive your protein of interest.

    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    100 mM NaCL, 20 mM Hepes, 10% glycerol. pH value is at the discretion of the manufacturer.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -80 °C
    Storage Comment
    Store at -80°C.
    Expiry Date
    Unlimited (if stored properly)
  • Target
    GALNT11 (UDP-N-Acetyl-alpha-D-Galactosamine:polypeptide N-Acetylgalactosaminyltransferase 11 (GalNAc-T11) (GALNT11))
    Alternative Name
    GALNT11 (GALNT11 Products)
    Synonyms
    A430075I06Rik Protein, AI648252 Protein, E430002F06Rik Protein, GALNACT11 Protein, polypeptide N-acetylgalactosaminyltransferase 11 Protein, Galnt11 Protein, GALNT11 Protein
    Background
    Polypeptide N-acetylgalactosaminyltransferase that catalyzes the initiation of protein O-linked glycosylation and is involved in left/right asymmetry by mediating O-glycosylation of NOTCH1. O-glycosylation of NOTCH1 promotes activation of NOTCH1, modulating the balance between motile and immotile (sensory) cilia at the left-right organiser (LRO). Polypeptide N-acetylgalactosaminyltransferases catalyze the transfer of an N-acetyl-D-galactosamine residue to a serine or threonine residue on the protein receptor. Displays the same enzyme activity toward MUC1, MUC4, and EA2 than GALNT1. Not involved in glycosylation of erythropoietin (EPO). {ECO:0000269|PubMed:11925450, ECO:0000269|PubMed:24226769}.
    Molecular Weight
    66.5 kDa Including tag.
    UniProt
    Q8NCW6
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