IQCF1 antibody (Biotin)

Catalog No. ABIN1400401

This Rabbit Polyclonal antibody specifically detects IQCF1 in WB and IHC (p). It exhibits reactivity toward Human.

Quick Overview for IQCF1 antibody (Biotin) (ABIN1400401)

Target: IQCF1 (IQ Motif Containing F1 (IQCF1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This IQCF1 antibody is conjugated to Biotin

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-IQCF1 Antibody (Biotin)

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human IQCF1

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

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

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for IQCF1

Target: IQCF1 (IQ Motif Containing F1 (IQCF1))

Alternative Name: IQCF1

Background:

Synonyms: IQ domain-containing protein F1, IQ mot containing F1, Iqcf1, IQCF1_HUMAN, MGC39725.

Background: IQCF1 is an 81 amino acid protein encoded by the IQCF1 gene, which maps to human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

Gene ID: 132141