EFR3A antibody

Catalog No. ABIN1385455

Product Details anti-EFR3A Antibody

Target: EFR3A (EFR3 Homolog A (EFR3A))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This EFR3A antibody is un-conjugated

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

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human EFR3A

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

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

Storage: 4 °C,-20 °C

Storage Comment: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for EFR3A

Target: EFR3A (EFR3 Homolog A (EFR3A))

Alternative Name: EFR3A (EFR3A Products)

Synonyms: RGD1305976 antibody, A130089M23Rik antibody, BB071175 antibody, C76891 antibody, C920006C10Rik antibody, D030063F01Rik antibody, mKIAA0143 antibody, EFR3 homolog A antibody, EFR3 homolog A L homeolog antibody, Efr3a antibody, EFR3A antibody, efr3a.L antibody

Background:

Synonyms: EFR 3A, EFR3 homolog A S. cerevisiae, EFR3 homolog A, KIAA0143, Protein EFR3 homolog A, Protein EFR3 like,

Background: EFR3A is a plasma membrane protein that contains 821 amino acids and belongs to the EFR3 family. EFR3A is alternatively spliced creating three isoforms and is encoded by a gene that maps to human chromosome 8. Human chromosome 8 consists of nearly 146 million base pairs, encodes over 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.

Gene ID: 23167