HEMK1 antibody (AA 21-120) (HRP)

Catalog No. ABIN1711575

This anti-HEMK1 antibody is a Rabbit Polyclonal antibody detecting HEMK1 in WB and ELISA. Suitable for Mouse.

Quick Overview for HEMK1 antibody (AA 21-120) (HRP) (ABIN1711575)

Target: HEMK1 (HemK Methyltransferase Family Member 1 (HEMK1))

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HEMK1 antibody is conjugated to HRP

Application: Western Blotting (WB), ELISA

Product Details anti-HEMK1 Antibody (HRP)

Binding Specificity: AA 21-120

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Dog,Cow,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human HEMK1

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000

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.

Handling Advice: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

Storage: -20 °C

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

Expiry Date: 12 months

Target Details for HEMK1

Target: HEMK1 (HemK Methyltransferase Family Member 1 (HEMK1))

Alternative Name: HEMK1

Background:

Synonyms: HEMK, HemK methyltransferase family member 1, Hemk1, HEMK1_HUMAN, M.HsaHemKP, MTQ1.

Background: HEMK1 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. name change

Gene ID: 51409