KCNJ13 antibody (N-Term)

Catalog No. ABIN656321

The Rabbit Polyclonal anti-KCNJ13 antibody is suitable to detect KCNJ13 in samples from Human. It has been validated for WB and IHC (p).

Quick Overview for KCNJ13 antibody (N-Term) (ABIN656321)

Target: KCNJ13 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 13 (KCNJ13))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This KCNJ13 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: RB31344

Product Details anti-KCNJ13 Antibody

Binding Specificity: AA 67-95, N-Term

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This KCNJ13 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 67-95 amino acids from the N-terminal region of human KCNJ13.

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000. WB: 1:2000. IHC-P: 1:10~50

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Storage Comment: KCNJ13 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Expiry Date: 6 months

Target Details for KCNJ13

Target: KCNJ13 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 13 (KCNJ13))

Alternative Name: KCNJ13

Background: This gene encodes a member of the inwardly rectifying potassium channel family of proteins. Members of this family form ion channel pores that allow potassium ions to pass into a cell. The encoded protein belongs to a subfamily of low signal channel conductance proteins that have a low dependence on potassium concentration. Mutations in this gene are associated with snowflake vitreoretinal degeneration. Alternate splicing results in multiple transcript variants.

Molecular Weight: 40530

Gene ID: 3769

NCBI Accession: NP_001165887, NP_001165888, NP_002233

UniProt: O60928