PCDH21 antibody (AA 20-300)
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- Target See all PCDH21 (PCDH24) Antibodies
- PCDH21 (PCDH24) (Protocadherin 21 (PCDH24))
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Binding Specificity
- AA 20-300
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This PCDH21 antibody is un-conjugated
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Application
- Western Blotting (WB)
- Purpose
- CDHR1 Rabbit pAb
- Sequence
- QANFAPHFFD NGVGSTNGNM ALFSLPEDTP VGSHVYTLNG TDPEGDPISY HISFDPSTRS VFSVDPTFGN ITLVEELDRE REDEIEAIIS ISDGLNLVAE KVVILVTDAN DEAPRFIQEP YVALVPEDIP AGSIIFKVHA VDRDTGSGGS VTYFLQNLHS PFAVDRHSGV LRLQAGATLD YERSRTHYIT VVAKDGGGRL HGADVVFSAT TTVTVNVEDV QDMAPVFVGT PYYGYVYEDT LPGSEVLKVV AMDGDRGKPN RILYSLVNGN DGAFEINETS G
- Cross-Reactivity
- Human, Mouse, Rat
- Characteristics
- Polyclonal Antibodies
- Purification
- Affinity purification
- Immunogen
- Recombinant fusion protein containing a sequence corresponding to amino acids 20-300 of human CDHR1 (NP_001165442.1).
- Isotype
- IgG
- Top Product
- Discover our top product PCDH24 Primary Antibody
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- Application Notes
- WB,1:500 - 1:2000
- Restrictions
- For Research Use only
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- Format
- Liquid
- 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
- PCDH21 (PCDH24) (Protocadherin 21 (PCDH24))
- Alternative Name
- CDHR1 (PCDH24 Products)
- Synonyms
- CORD15 antibody, PCDH21 antibody, PRCAD antibody, RP65 antibody, Pcdh21 antibody, Prcad antibody, mKIAA1775 antibody, prCAD antibody, pcdh21 antibody, cadherin related family member 1 antibody, cadherin-related family member 1 antibody, cadherin related family member 1 L homeolog antibody, CDHR1 antibody, Cdhr1 antibody, cdhr1.L antibody
- Background
- This gene belongs to the cadherin superfamily of calcium-dependent cell adhesion molecules. The encoded protein is a photoreceptor-specific cadherin that plays a role in outer segment disc morphogenesis. Mutations in this gene are associated with inherited retinal dystrophies. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2013],CORD15,PCDH21,PRCAD,RP65,CDHR1,Signal Transduction,Cell Biology & Developmental Biology,Cell Adhesion,Cadherins,Cytoskeleton,Neuroscience,Calcium Signaling,CDHR1
- Gene ID
- 92211
- UniProt
- Q96JP9
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