RDH5 polyclonal antibody

Catalog # PAB19051

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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)

RDH5 polyclonal antibody (Cat # PAB19051) (2 ug/mL) staining of mouse eye lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.

  • Specification

    Product Description

    Goat polyclonal antibody raised against synthetic peptide of RDH5.

    Immunogen

    A synthetic peptide corresponding to amino acids 19-31 at internal region of human RDH5.

    Sequence

    C-RDRQSLPASNAFV

    Host

    Goat

    Theoretical MW (kDa)

    35

    Reactivity

    Mouse

    Form

    Liquid

    Purification

    Antigen affinity purification

    Concentration

    0.5 mg/mL

    Recommend Usage

    ELISA (1:8000)
    Western Blot (2-4 ug/mL)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In Tris saline, pH7.3 (0.5% BSA, 0.02% sodium azide)

    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)

    RDH5 polyclonal antibody (Cat # PAB19051) (2 ug/mL) staining of mouse eye lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.

    Enzyme-linked Immunoabsorbent Assay

  • Gene Info — RDH5

    Entrez GeneID

    5959

    Protein Accession#

    NP_002896.2

    Gene Name

    RDH5

    Gene Alias

    FLJ39337, FLJ97089, HSD17B9, RDH1, SDR9C5

    Gene Description

    retinol dehydrogenase 5 (11-cis/9-cis)

    Omim ID

    136880 601617

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases (SDR) family. This retinol dehydrogenase functions to catalyze the final step in the biosynthesis of 11-cis retinaldehyde, which is the universal chromophore of visual pigments. Mutations in this gene cause autosomal recessive fundus albipunctatus, a rare form of night blindness that is characterized by a delay in the regeneration of cone and rod photopigments. [provided by RefSeq

    Other Designations

    11-cis RDH|9-cis-retinol specific dehydrogenase|retinol dehydrogenase 1|retinol dehydrogenase 5 (11-cis and 9-cis)|short chain dehydrogenase/reductase family 9C, 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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