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, ELISA and IHC.

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, Immunohistochemistry (IHC)

Product Details anti-KCTD7 Antibody

Binding Specificity: AA 181-230

Purpose: Rabbit Anti-KCTD7 Polyclonal Antibody

Specificity: This antibody detects endogenous levels of KCTD7

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-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 1:500-2000,IHC 1:50-300,ELISA 1:2000-20000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

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.

Expiry Date: 12 months

Target Details for KCTD7

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

Alternative Name: KCTD7

Background: BTB/POZ domain-containing protein KCTD7KCTD7 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.

Molecular Weight: 33kD

Gene ID: 154881

UniProt: Q96MP8