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CLN5 antibody (C-Term)
CLN5
Reactivity: Human, Rat, Cow, Dog, Guinea Pig, Horse, Pig, Rabbit
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-CLN5 Antibody
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Target
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CLN5
(Ceroid-Lipofuscinosis, Neuronal 5 (CLN5))
Binding Specificity
All epitopes for CLN5 antibodies
C-Term
Reactivity
Human, Rat, Cow, Dog, Guinea Pig, Horse, Pig, Rabbit
Host
All hosts for CLN5 antibodies
Rabbit
Clonality
All clonalities for CLN5 antibodies
Polyclonal
Conjugate
All conjugates for CLN5 antibodies
This CLN5 antibody is un-conjugated
Application
Please inquire
Sequence
DNETGIYYET WNVKASPEKG AETWFDSYDC SKFVLRTFNK LAEFGAEFKN
Predicted Reactivity
Cow: 77%, Dog: 79%, Guinea Pig: 79%, Horse: 86%, Human: 100%, Pig: 86%, Rabbit: 86%, Rat: 79%
Purification
Affinity purified
Immunogen
The immunogen is a synthetic peptide directed towards the C terminal region of human CLN5
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Discover our top product CLN5 Primary Antibody
Alternatives
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Application Details
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Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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
For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
Target Details for CLN5
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Target
CLN5
(Ceroid-Lipofuscinosis, Neuronal 5 (CLN5))
Alternative Name
CLN5 (CLN5 Products )
Synonyms
NCL antibody, A730075N08Rik antibody, CLN5, intracellular trafficking protein antibody, ceroid-lipofuscinosis, neuronal 5 antibody, CLN5 antibody, Cln5 antibody
Background
This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function. Alias Symbols: NCL Protein Interaction Partner: ARHGAP36, FBXO27, SPNS1, SFXN3, SLC25A22, SEC61A1, FBXO6, PHGDH, GANAB, OS9, CDIPT, SLC25A13, CDS2, SLC25A11, XPO1, SLC25A1, SEL1L, RPN1, RCN2, HMGCS1, DBH, CLN5, CLGN, CANX, CALU, CALR, ATP2A2, ATP1A3, ARF4, SLC25A6, SLC25A5, SLC25A4, Dlg4, UBC, KRT8, Protein Size: 358
Gene ID
1203
NCBI Accession
NM_006493 , NP_006484
UniProt
O75503
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