WNT9B polyclonal antibody
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More Files
- More Functions
Western Blot (Tissue lysate)
WNT9B polyclonal antibody (Cat # PAB16632) (0.3 ug/mL) staining of human brain cerebellum lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
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Specification
Product Description
Goat polyclonal antibody raised against synthetic peptide of WNT9B.
Immunogen
A synthetic peptide corresponding to amino acids at internal region of human WNT9B.
Sequence
C-KRGNKDLRARADA
Host
Goat
Theoretical MW (kDa)
39
Reactivity
Human
Form
Liquid
Purification
Antigen affinity purification
Concentration
0.5 mg/mL
Recommend Usage
ELISA (1:8000)
Western Blot (0.3-1 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
Storage Instruction
Store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Tissue lysate)
WNT9B polyclonal antibody (Cat # PAB16632) (0.3 ug/mL) staining of human brain cerebellum lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.Enzyme-linked Immunoabsorbent Assay
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Gene Info — WNT9B
Entrez GeneID
7484Protein Accession#
NP_003387.1Gene Name
WNT9B
Gene Alias
WNT14B, WNT15
Gene Description
wingless-type MMTV integration site family, member 9B
Omim ID
602864Gene Ontology
HyperlinkGene Summary
The WNT gene family 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 a member of the WNT gene family. Study of its expression in the teratocarcinoma cell line NT2 suggests that it may be implicated in the early process of neuronal differentiation of NT2 cells induced by retinoic acid. This gene is clustered with WNT3, another family member, in the chromosome 17q21 region. [provided by RefSeq
Other Designations
wingless-type MMTV integration site family, member 15
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Interactome
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Pathway
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Disease
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Publication Reference
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Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate.
Chiquet BT, Blanton SH, Burt A, Ma D, Stal S, Mulliken JB, Hecht JT.
Human Molecular Genetics 2008 Jul; 17(14):2212.
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Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate.
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