SCN2B antibody (AA 30-160)

Catalog No. ABIN6147437

This Rabbit Polyclonal antibody specifically detects SCN2B in WB. It exhibits reactivity toward Human.

Quick Overview for SCN2B antibody (AA 30-160) (ABIN6147437)

Target: SCN2B (Sodium Channel, Voltage-Gated, Type II, beta (SCN2B))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SCN2B antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-SCN2B Antibody

Binding Specificity: AA 30-160

Sequence: MEVTVPATLN VLNGSDARLP CTFNSCYTVN HKQFSLNWTY QECNNCSEEM FLQFRMKIIN LKLERFQDRV EFSGNPSKYD VSVMLRNVQP EDEGIYNCYI MNPPDRHRGH GKIHLQVLME EPPERDSTVA V

Cross-Reactivity: Human

Characteristics: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 30-160 of human SCN2B (NP_004579.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

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: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for SCN2B

Target: SCN2B (Sodium Channel, Voltage-Gated, Type II, beta (SCN2B))

Alternative Name: SCN2B

Background: The protein encoded by this gene is the beta 2 subunit of the type II voltage-gated sodium channel. The encoded protein is involved in cell-cell adhesion and cell migration. Defects in this gene can be a cause of Brugada Syndrome, atrial fibrillation, or sudden infant death syndrome.,SCN2B,ATFB14,Neuroscience,SCN2B

Molecular Weight: 24 kDa

Gene ID: 6327

UniProt: O60939