Chromosome 5 Open Reading Frame 39 (C5orf39) antibody
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- Target See all Chromosome 5 Open Reading Frame 39 (C5orf39) Antibodies
- Chromosome 5 Open Reading Frame 39 (C5orf39)
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- Un-conjugated
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Application
- ELISA, Immunohistochemistry (IHC)
- Cross-Reactivity
- Human
- Purification
- Antigen affinity purification
- Immunogen
- Synthetic peptide of Human ANXA2R
- Isotype
- IgG
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anti-Chromosome 5 Open Reading Frame 39 (C5orf39) (AA 1-193) antibody
C5orf39 Reactivity: Human WB Host: Mouse Polyclonal unconjugated
anti-Chromosome 5 Open Reading Frame 39 (C5orf39) (N-Term) antibodyC5orf39 Reactivity: Human, Monkey WB Host: Rabbit Polyclonal unconjugated
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- Application Notes
- ELISA:1:1000-1:2000, IHC:1:25-1:100,
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
- 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,-80 °C
- Storage Comment
- Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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- Target
- Chromosome 5 Open Reading Frame 39 (C5orf39)
- Alternative Name
- ANXA2R (C5orf39 Products)
- Synonyms
- AX2R antibody, AXIIR antibody, C5orf39 antibody, annexin A2 receptor antibody, ANXA2R antibody
- Background
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Background: ANXA2R (annexin-2 receptor), also known as AX2R or C5orf39, is a 193 amino acid protein that is widely expressed and may act as an annexin II receptor on marrow stromal cells to induce osteoclast formation. In addition, ANXA2R is highly expressed in lymphocytes and is also found in resting CD4+ and CD8+ T cells. The gene encoding ANXA2R maps to human chromosome 5, which contains 181 million base pairs and comprises nearly 6 % of the human genome. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5-associated and is caused by insertions or deletions within the TCOF1 gene.
Aliases: Annexin 2 receptor antibody, Annexin II receptor antibody, Annexin-2 receptor antibody, ANXA2R antibody, AX2R antibody, AX2R_HUMAN antibody, AXIIR antibody, C5orf39 antibody, Chromosome 5 open reading frame 39 antibody, LOC389289 antibody
- UniProt
- Q3ZCQ2
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