All products Antibodies Rabbit anti-IKBKG polyclonal antibody - middle region

Rabbit anti-IKBKG polyclonal antibody - middle region

Catalog Number:OM105096

  • Lanes:
    1. 100 ug mouse testis lysate
    2. 100 ug HeLa cell lysate
    Primary Antibody Dilution:
    1:800
    Secondary Antibody:
    Anti-rabbit-AP
    Secondary Antibody Dilution:
    1:10000
    Gene Name:
    IKBKG
    Submitted by:
    Andreia Carvalho, Instituto de Biologia Molecular e Celular, Universidade do Porto (IBMC-UP)/Organelle Biogenesis and Function (OBF) Group

  • WB Suggested Anti-IKBKG Antibody Titration: 1.25ug/ml
    ELISA Titer: 1:312500
    Positive Control: HepG2 cell lysate

    IKBKG is strongly supported by BioGPS gene expression data to be expressed in Human HepG2 cells

Product Profile

Product Name Rabbit anti-IKBKG polyclonal antibody - middle region
Antibody Type Primary Antibodies
Immunogen
The immunogen for anti-IKBKG antibody: synthetic peptide directed towards the middle region of human IKBKG

Key Feature

Clonality Polyclonal
Isotype IgG
Host Species Rabbit
Tested Applications

WB

WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
Species Reactivity

DogGuinea PigHorseHumanMousePigRabbitRat

Concentration 1 mg/ml
Purification Protein A

Target Information

Gene Symbol IKBKG
Gene Synonyms
IKBKG
Gene Full Name Inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
Gene Summary
Familial incontinentia pigmenti (IP) is a genodermatosis that segregates as an X-linked dominant disorder and is usually lethal prenatally in males . In affected females it causes highly variable abnormalities of the skin, hair, nails, teeth, eyes, and central nervous system. The prominent skin signs occur in 4 classic cutaneous stages: perinatal inflammatory vesicles, verrucous patches, a distinctive pattern of hyperpigmentation, and dermal scarring. Cells expressing the mutated X chromosome are eliminated selectively around the time of birth, so females with IP exhibit extremely skewed X-inactivation. Familial incontinentia pigmenti is caused by mutations in the NEMO gene and is here referred to as IP2, or 'classical' incontinentia pigmenti. Sporadic incontinentia pigmenti, the so-called IP1, which maps to Xp11, is categorized as hypomelanosis of Ito
Alternative Names
IP
IP1
IP2
FIP3
IPD2
NEMO
FIP-3
Fip3p
AMCBX1
IKK-gamma
Molecular Weight(MW) 48kDa
Sequence 419 amino acids

Database Links

Entrez Gene 8517
SwissProt ID Q9Y6K9
Protein Accession NP_003630

Application

  • Application

    Lanes:
    1. 100 ug mouse testis lysate
    2. 100 ug HeLa cell lysate
    Primary Antibody Dilution:
    1:800
    Secondary Antibody:
    Anti-rabbit-AP
    Secondary Antibody Dilution:
    1:10000
    Gene Name:
    IKBKG
    Submitted by:
    Andreia Carvalho, Instituto de Biologia Molecular e Celular, Universidade do Porto (IBMC-UP)/Organelle Biogenesis and Function (OBF) Group

  • Application

    WB Suggested Anti-IKBKG Antibody Titration: 1.25ug/ml
    ELISA Titer: 1:312500
    Positive Control: HepG2 cell lysate

    IKBKG is strongly supported by BioGPS gene expression data to be expressed in Human HepG2 cells

Application Notes
WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.

Additional Information

Form Liquid
Storage Instructions Aliquot and store at -20°C. Avoid repeated freeze / thaw cycles
Storage Buffer phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Note: The product is for research use only,not for use in diagnostic or therapeutic procedures.

  • Catalog Number: OM105096
  • Price: $336.00
  • Discount Price
  • Size:
  • Store: In stock
  • Lead time: 2~3 Week
  • Quantity:
    - +
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