SMYD2A antibody

Catalog No. ABIN715571

The Rabbit Polyclonal anti-SMYD2A antibody is suitable to detect SMYD2A in samples from Human. It has been validated for WB, IF, IHC (p) and IHC (fro).

Quick Overview for SMYD2A antibody (ABIN715571)

Target: SMYD2A (SET and MYND Domain Containing 2a (SMYD2A))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SMYD2A antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Product Details anti-SMYD2A Antibody

Purpose: SMYD2 Polyclonal Antibody

Cross-Reactivity: Mouse, Rat

Predicted Reactivity: Human,Dog,Cow,Pig

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human SMYD2

Isotype: IgG

Application Details

Application Notes: WB(1:500-2000), IHC-P(1:100-500), IHC-F(1:100-500), IF(1:100-500)

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Storage Comment: Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for SMYD2A

Target: SMYD2A (SET and MYND Domain Containing 2a (SMYD2A))

Alternative Name: SMYD2

Background:

Synonyms: HSKM B, HSKM-B, HSKMB, Histone methyltransferase SMYD2, HSKM-B, Lysine N-methyltransferase 3C, MGC119305, N lysine methyltransferase SMYD2, N-lysine methyltransferase SMYD2, SET and MYND domain containing 2, SET and MYND domain containing protein 2, SET and MYND domain-containing protein 2, Smyd2, SMYD2_HUMAN, Zinc finger MYND domain containing 14, ZMYND14.

Background: This gene encodes the type I intermediate filament chain keratin 17, expressed in nail bed, hair follicle, sebaceous glands, and other epidermal appendages. Mutations in this gene lead to Jackson-Lawler type pachyonychia congenita and steatocystoma multiplex. [provided by RefSeq, Aug 2008]

Gene ID: 56950

UniProt: Q9NRG4