C7orf45 antibody (AA 51-150) (Biotin)
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- Target See all C7orf45 (SSMEM1) products
- C7orf45 (SSMEM1) (Serine-Rich Single-Pass Membrane Protein 1 (SSMEM1))
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Binding Specificity
- AA 51-150
- Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This C7orf45 antibody is conjugated to Biotin
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Application
- ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Predicted Reactivity
- Human,Mouse
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C7orf45
- Isotype
- IgG
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- Application Notes
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IHC-P 1:200-400
IHC-F 1:100-500 - 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
- C7orf45 (SSMEM1) (Serine-Rich Single-Pass Membrane Protein 1 (SSMEM1))
- Alternative Name
- C7orf45 (SSMEM1 Products)
- Synonyms
- C7orf45 antibody, RGD1559502 antibody, 1700016K02Rik antibody, 1700025E21Rik antibody, serine rich single-pass membrane protein 1 antibody, serine-rich single-pass membrane protein 1 antibody, SSMEM1 antibody, Ssmem1 antibody
- Background
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Synonyms: C7orf45, CG045_HUMAN, chromosome 7 open reading frame 45, FLJ40316, Uncharacterized protein C7orf45.
Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf45 gene product has been provisionally designated C7orf45 pending further characterization.
- Gene ID
- 136263
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