FLCN Polyclonal Antibody, APC Conjugated

Product Specifications

Background

This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in three transcript variants encoding different isoforms.

Synonyms

BHD; BHD skin lesion fibrofolliculoma protein; Birt Hogg Dube syndrome protein; FLCL; Folliculin; FLCN_HUMAN.

Gene ID

201163

Cellular Locus

Cytoplasm, Nucleus

Host

Rabbit

Immunogen

65-165/579

Target

FLCN

Clonality

Polyclonal

Isotype

IgG

Conjugation

APC

Source

KLH conjugated synthetic peptide derived from human Folliculin

Applications

IF (IHC-P), IF (IHC-F), IF (ICC)

Purification

Purified by Protein A.

Excitation Emission

650nm/660nm

Concentration

1µg/µl

Dilution

IF (IHC-P) (1:50-200), IF (IHC-F) (1:50-200), IF (ICC) (1:50-200)

Buffer

Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Modification

Unmodified

Storage Conditions

Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Gene ID URL

201163

Predicted Cross Reactivity

Human, Mouse, Rat, Dog, Cow, Sheep, Horse, Chicken

Curated Selection

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