SOX9 monoclonal antibody, clone 1B11

Catalog # MAB17870

Size

Price

Stock

Quantity

Size:100 ug
Price: USD $ 531.00
Stock:
order now, ship in 5 days
abnova-minus
abnova-plus

* The price is valid only in USA. Please select country.

Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Enzyme-linked Immunoabsorbent Assay
Application

Enzyme-linked Immunoabsorbent Assay

ELISA analysis with SOX9 monoclonal antibody, clone 1B11 (Cat # MAB17870).

  • Specification

    Product Description

    Mouse monoclonal antibody raised against partial recombinant human SOX9.

    Immunogen

    Recombinant protein corresponding to amino acids 147-306 of human SOX9.

    Host

    Mouse

    Theoretical MW (kDa)

    56

    Reactivity

    Human

    Form

    Liquid

    Isotype

    IgG1

    Recommend Usage

    ELISA (1:10000)
    Immunofluorescence (1:200-1:1000)
    Western Blot (1:100-1:500)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS (0.05% sodium azide).

    Storage Instruction

    Store at 4°C. For long term storage 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

    Immunofluorescence

    Enzyme-linked Immunoabsorbent Assay

    ELISA analysis with SOX9 monoclonal antibody, clone 1B11 (Cat # MAB17870).
  • Gene Info — SOX9

    Entrez GeneID

    6662

    Protein Accession#

    P48436

    Gene Name

    SOX9

    Gene Alias

    CMD1, CMPD1, SRA1

    Gene Description

    SRY (sex determining region Y)-box 9

    Omim ID

    114290 608160

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene recognizes the sequence CCTTGAG along with other members of the HMG-box class DNA-binding proteins. It acts during chondrocyte differentiation and, with steroidogenic factor 1, regulates transcription of the anti-Muellerian hormone (AMH) gene. Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia, frequently with sex reversal. [provided by RefSeq

    Other Designations

    SRY (sex determining region Y)-box 9 (campomelic dysplasia, autosomal sex-reversal)|SRY (sex-determining region Y)-box 9 (campomelic dysplasia, autosomal sex-reversal)|SRY (sex-determining region Y)-box 9 protein|campomelic dysplasia, autosomal sex-revers

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
4 Products to Compare
Remove All