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 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 |
Clonality | Polyclonal |
---|---|
Isotype | IgG |
Host Species | Rabbit |
Tested Applications | |
WB:1:500~1:2000 Notes:Optimal dilutions/concentrations should be determined by the researcher. |
|
Species Reactivity | |
Concentration | 1 mg/ml |
Purification | Protein A |
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 |
Entrez Gene | 8517 |
---|---|
SwissProt ID | Q9Y6K9 |
Protein Accession | NP_003630 |
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
Application Notes | WB:1:500~1:2000 Notes:Optimal dilutions/concentrations should be determined by the researcher. |
---|
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. |
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