WNT7A antibody
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- Target See all WNT7A Antibodies
- WNT7A (Wingless-Type MMTV Integration Site Family, Member 7A (WNT7A))
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Reactivity
- Human, Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This WNT7A antibody is un-conjugated
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Application
- Western Blotting (WB), Immunofluorescence (IF)
- Characteristics
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogen
- Recombinant fusion protein of human WNT7A (NP_004616.2).
- Isotype
- IgG
- Top Product
- Discover our top product WNT7A Primary Antibody
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- Application Notes
- WB 1:500-1:2000 IF 1:10-1:100
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 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
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- WNT7A (Wingless-Type MMTV Integration Site Family, Member 7A (WNT7A))
- Alternative Name
- WNT7A (WNT7A Products)
- Synonyms
- wnt7a antibody, AI849442 antibody, Wnt-7a antibody, px antibody, tw antibody, Xwnt-7a antibody, wnt-7a antibody, wnt7a-A antibody, Wnt family member 7A antibody, wingless-type MMTV integration site family, member 7Aa antibody, wingless-type MMTV integration site family, member 7A antibody, wingless-type MMTV integration site family member 7A S homeolog antibody, WNT7A antibody, wnt7aa antibody, Wnt7a antibody, wnt7a.S antibody
- Background
- This gene is a member of the WNT gene family, which consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is involved in the development of the anterior-posterior axis in the female reproductive tract, and also plays a critical role in uterine smooth muscle pattering and maintenance of adult uterine function. Mutations in this gene are associated with Fuhrmann and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromes.
- Molecular Weight
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Observed_MW: 39 kDa
Calculated_MW: 39 kDa
- Gene ID
- 7476
- UniProt
- O00755
- Pathways
- WNT Signaling, Stem Cell Maintenance, Asymmetric Protein Localization
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