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Key Product Details

Species Reactivity

Human

Applications

Flow Cytometry, Western Blot

Label

Unconjugated

Antibody Source

Monoclonal Mouse IgG1 Clone # 46B844

Format

Azide Free

Concentration

0.5 mg/ml

Product Specifications

Immunogen

Full-length human IKK gamma protein.

Clonality

Monoclonal

Host

Mouse

Isotype

IgG1

Scientific Data Images for IKK gamma Antibody (46B844) - Azide Free

Western Blot: IKK gamma Antibody (46B844)Azide Free [NBP2-33220]

Western Blot: IKK gamma Antibody (46B844)Azide Free [NBP2-33220]

Western Blot: IKK gamma Antibody (46B844) - Azide Free [NBP2-33220] - Analysis using NEMO (IKKgamma) antibody. Lysate from human Jurkat cells probed with NEMO antibody at 2 ug/ml. The goat anti-mouse IgG1 HRP secondary and PicoTect ECL substrate solution were used for this test. Image from the standard format of this antibody.
Flow Cytometry: IKK gamma Antibody (46B844) - Azide Free [NBP2-33220]

Flow Cytometry: IKK gamma Antibody (46B844) - Azide Free [NBP2-33220]

Flow Cytometry: IKK gamma Antibody (46B844) - Azide Free [NBP2-33220] - Human Jurkat cells were probed using 0.1 ug of NEMO antibody (red) and 0.1 ug of isotype control (green), with shaded histogram representing cells alone and an anti-mouse IgG-FITC secondary antibody. Image from the standard format of this antibody.

Applications for IKK gamma Antibody (46B844) - Azide Free

Application
Recommended Usage

Flow Cytometry

1ul/1 million cells

Western Blot

2 ug/ml
Application Notes
A 48 kDa band is observed.
Please Note: Optimal dilutions of this antibody should be experimentally determined.

Formulation, Preparation, and Storage

Purification

Protein G purified

Formulation

PBS - BSA free

Format

Azide Free

Preservative

No Preservative

Concentration

0.5 mg/ml

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.

Background: IKK gamma

Familial incontinentia pigmenti (IP) is a genodermatosis that segregates as an X-linked dominant disorder and is usually lethal prenatally in males (The International Incontinentia Pigmenti Consortium, 2000 [PubMed 10839543]). 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 (MIM 300337).[supplied by OMIM]

Long Name

IkB Kinase gamma

Alternate Names

FIP3P, IKBKG, IKKAP1, NEMO

Gene Symbol

IKBKG

Additional IKK gamma Products

Product Documents for IKK gamma Antibody (46B844) - Azide Free

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot number in the search box below.

Product Specific Notices for IKK gamma Antibody (46B844) - Azide Free

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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