FUNDC2 antibody

Catalog No. ABIN7246850

The Rabbit Polyclonal anti-FUNDC2 antibody has been validated for ELISA and IHC. It is suitable to detect FUNDC2 in samples from Human.

Quick Overview for FUNDC2 antibody (ABIN7246850)

Target: FUNDC2 (FUN14 Domain Containing 2 (FUNDC2))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FUNDC2 antibody is un-conjugated

Application: ELISA, Immunohistochemistry (IHC)

Product Details anti-FUNDC2 Antibody

Characteristics: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogen: Fusion protein of human FUNDC2

Isotype: IgG

Application Details

Application Notes: IHC 1:50-1:300, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.72 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for FUNDC2

Target: FUNDC2 (FUN14 Domain Containing 2 (FUNDC2))

Alternative Name: FUNDC2

Background: FUNDC2 (FUN14 domain-containing protein 2), also known as HCC-3 (cervical cancer proto-oncogene 3 protein), HCBP6 (hepatitis C virus core-binding protein 6) or DC44, is a 189 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC2 maps to human chromosome Xq28. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

UniProt: Q9BWH2