EFR3A antibody (Biotin)
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- Target See all EFR3A Antibodies
- EFR3A (EFR3 Homolog A (EFR3A))
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This EFR3A antibody is conjugated to Biotin
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Application
- Western Blotting (WB), 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
- Top Product
- Discover our top product EFR3A Primary Antibody
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- Application Notes
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WB 1:300-5000
IHC-P 1:200-400 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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
- -20 °C
- Storage Comment
- Store at -20°C for 12 months.
- Expiry Date
- 12 months
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- 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
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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
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