TM9SF4 antibody (AA 101-200) (Cy5)

Catalog No. ABIN1416336

This anti-TM9SF4 antibody is a Rabbit Polyclonal antibody detecting TM9SF4 in WB, IF (cc), IF (p). Suitable for Mouse.

Quick Overview for TM9SF4 antibody (AA 101-200) (Cy5) (ABIN1416336)

Target: TM9SF4 (Transmembrane 9 Superfamily Protein Member 4 (TM9SF4))

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TM9SF4 antibody is conjugated to Cy5

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-TM9SF4 Antibody (Cy5)

Binding Specificity: AA 101-200

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human TM9SF4

Isotype: IgG

Application Details

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

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for TM9SF4

Target: TM9SF4 (Transmembrane 9 Superfamily Protein Member 4 (TM9SF4))

Alternative Name: TM9SF4

Background:

Synonyms: dJ836N17.2, Transmembrane 9 superfamily member 4, TM9SF4, KIAA0255

Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis which are thought important for seminal production and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20.

Gene ID: 9777

UniProt: Q92544