KCTD7 antibody (AA 181-230)

Catalog No. ABIN7229266

The Rabbit Polyclonal anti-KCTD7 antibody is suitable to detect KCTD7 in samples from Human, Mouse and Rat. It has been validated for WB and ELISA.

Quick Overview for KCTD7 antibody (AA 181-230) (ABIN7229266)

Target: KCTD7 (Potassium Channel Tetramerisation Domain Containing 7 (KCTD7))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This KCTD7 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-KCTD7 Antibody

Binding Specificity: AA 181-230

Purpose: KCTD7 Polyclonal Antibody

Specificity: This antibody detects endogenous levels of KCTD7

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogen: Synthesized peptide derived from part region of human KCTD7 protein at AA range: 181-230

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:10000-1:20000).

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol as stabilizer.

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Target Details for KCTD7

Target: KCTD7 (Potassium Channel Tetramerisation Domain Containing 7 (KCTD7))

Alternative Name: KCTD7

Background: Rabbit Anti-KCTD7 Polyclonal Antibody,BTB/POZ domain-containing protein KCTD7,KCTD7 encodes a member of the potassium channel tetramerization domain-containing protein family. Family members are identified on a structural basis and contain an amino-terminal domain similar to the T1 domain present in the voltage-gated potassium channel. Mutations in this gene have been associated with progressive myoclonic epilepsy-3. Alternative splicing results in multiple transcript variants.,KCTD7

Molecular Weight: observerd band 33kDa

Gene ID: 154881

UniProt: Q96MP8