SETD5 antibody (AA 196-1275)

Catalog No. ABIN7825811

The Rabbit Polyclonal anti-SETD5 antibody (ABIN7825811) specifically detects SETD5 in ELISA, WB and FACS. The antibody is reactive with Human samples.

Quick Overview for SETD5 antibody (AA 196-1275) (ABIN7825811)

Target: SETD5 (SET Domain Containing 5 (SETD5))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SETD5 antibody is un-conjugated

Application: ELISA, Western Blotting (WB), Flow Cytometry (FACS)

Product Details anti-SETD5 Antibody

Binding Specificity: AA 196-1275

Purpose: Anti-SETD5 Antibody

Cross-Reactivity (Details): No cross-reactivity with other proteins

Characteristics: Anti-SETD5 Antibody catalog # A10168. Tested in WB, Flow Cytometry, ELISA applications. This antibody reacts with Human. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human SETD5 recombinant protein (Position: Q196-R1275).

Isotype: IgG

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Human
Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human
ELISA, 0.1-0.5 μg/mL

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Storage: 4 °C,-20 °C

Storage Comment: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Target Details for SETD5

Target: SETD5 (SET Domain Containing 5 (SETD5))

Alternative Name: SETD5

Background: This function of this gene has yet to be determined but based on sequence similarity to other SET domain proteins it may function as a histone methyltransferase. Mutations in this gene have been associated with an autosomal dominant form of intellectual disability. Alternative splicing results in multiple transcript variants encoding different isoforms.

Molecular Weight: 160 kDa

Gene ID: 55209

UniProt: Q9C0A6