SLC17A5 polyclonal antibody

Catalog # PAB27673

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Price

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Quantity

Size:100 ug
Price: USD $ 428.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Western Blot (Tissue lysate)
Application

Western Blot (Tissue lysate)

SLC17A5 polycolnal antibody (Cat # PAB27673) (1ug/ml) staining of human placenta lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.

  • Specification

    Product Description

    Goat polyclonal antibody raised against synthetic peptide of SLC17A5.

    Immunogen

    A synthetic peptide corresponding to amino acids 85-99 at internal region of human SLC17A5.

    Sequence

    EHSAPIKVHHNQTGK

    Host

    Goat

    Theoretical MW (kDa)

    55-60

    Reactivity

    Human

    Purification

    Antigen affinity purification

    Concentration

    0.5 mg/mL

    Recommend Usage

    ELISA (1:128000)
    Western Blot (1-3ug/ml)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In Tris saline, pH 7.3 (0.02% sodium azide, 0.5% BSA)

    Storage Instruction

    Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Western Blot (Tissue lysate)

    SLC17A5 polycolnal antibody (Cat # PAB27673) (1ug/ml) staining of human placenta lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
  • Gene Info — SLC17A5

    Entrez GeneID

    26503

    Protein Accession#

    NP_036566.1

    Gene Name

    SLC17A5

    Gene Alias

    AST, FLJ22227, FLJ23268, ISSD, NSD, SD, SIALIN, SIASD, SLD

    Gene Description

    solute carrier family 17 (anion/sugar transporter), member 5

    Omim ID

    269920 604322 604369

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form. [provided by RefSeq

    Other Designations

    OTTHUMP00000016747|OTTHUMP00000039323|membrane glycoprotein HP59|sialic acid storage disease|sialin|solute carrier family 17, member 5

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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