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TRPC6 antibody
TRPC6
Reactivity: Human
IHC, ELISA
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-TRPC6 Antibody
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Target
See all TRPC6 Antibodies
TRPC6
(Transient Receptor Potential Cation Channel, Subfamily C, Member 6 (TRPC6))
Reactivity
All reactivities for TRPC6 antibodies
Human
Host
All hosts for TRPC6 antibodies
Rabbit
Clonality
All clonalities for TRPC6 antibodies
Polyclonal
Conjugate
All conjugates for TRPC6 antibodies
This TRPC6 antibody is un-conjugated
Application
All applications for TRPC6 antibodies
Immunohistochemistry (IHC), ELISA
Purification
Affinity purification
Immunogen
Synthetic peptide of human TRPC6
Isotype
IgG
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Discover our top product TRPC6 Primary Antibody
Alternatives
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Application Details
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Application Notes
IHC 1:50-1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.5 mg/mL
Buffer
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
Preservative
Sodium azide
Handling Advice
Avoid freeze / thaw cycles.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for TRPC6
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Target
TRPC6
(Transient Receptor Potential Cation Channel, Subfamily C, Member 6 (TRPC6))
Alternative Name
TRPC6 (TRPC6 Products )
Synonyms
FSGS2 antibody, TRP6 antibody, AV025995 antibody, LLHWJM002 antibody, LLHWJM003 antibody, LLHWJM004 antibody, TRP-6 antibody, Trrp6 antibody, mtrp6 antibody, trp6 antibody, bZ1P14.9 antibody, si:rp71-1p14.9 antibody, trpc6 antibody, transient receptor potential cation channel subfamily C member 6 antibody, transient receptor potential cation channel, subfamily C, member 6 antibody, transient receptor potential cation channel, subfamily C, member 6a antibody, TRPC6 antibody, Trpc6 antibody, trpc6a antibody, trpc6 antibody
Background
The protein encoded by this gene forms a receptor-activated calcium channel in the cell membrane. The channel is activated by diacylglycerol and is thought to be under the control of a phosphatidylinositol second messenger system. Activation of this channel occurs independently of protein kinase C and is not triggered by low levels of intracellular calcium. Defects in this gene are a cause of focal segmental glomerulosclerosis 2 (FSGS2).
NCBI Accession
NP_004612
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