Zbtb37 antibody

Instruction Manual!

Product name:	Zbtb37 antibody
Source:	Rabbit
Purity:	＞95%
Buffer Formulation:	phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Applications:	WB
Storage:	Aliquot and store at -20°C. Avoid repeated freeze / thaw cycles
UOM:	100ug

ProductName Rabbit anti-IKBKG polyclonal antibody - middle region

AntibodyType Primary Antibodies

Immunogen
The immunogen for anti-IKBKG antibody: synthetic peptide directed towards the middle region of human IKBKG

ProductName	Rabbit anti-IKBKG polyclonal antibody - middle region
AntibodyType	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

Species Reactivity
DogGuinea PigHorseHumanMousePigRabbitRat

Concentration 1mg/ml

Purification Protein A

Clonality	Polyclonal
Isotype	IgG
Host Species	Rabbit
Tested Applications	WB
Species Reactivity	DogGuinea PigHorseHumanMousePigRabbitRat
Concentration	1mg/ml
Purification	Protein A

Target Information

GeneSymbol IKBKG

GeneSynonyms
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
More

Alternative Names
IP
IP1
IP2
FIP3
IPD2
NEMO
FIP-3
Fip3p
AMCBX1
IKK-gamma
More

MolecularWeight(MW) 48kDa

Sequence 419 amino acids

GeneSymbol	IKBKG
GeneSynonyms	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 More
Alternative Names	IP IP1 IP2 FIP3 IPD2 NEMO FIP-3 Fip3p AMCBX1 IKK-gamma More
MolecularWeight(MW)	48kDa
Sequence	419 amino acids

Database Links

Entrez Gene 8517

SwissProt ID Q9Y6K9

Protein Accession NP_003630

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

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.

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.