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WBSCR16 antibody (AA 1-230)
WBSCR16
Reactivity: Human
WB
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-WBSCR16 Antibody
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Target
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WBSCR16
(Williams-Beuren Syndrome Chromosome Region 16 (WBSCR16))
Binding Specificity
All epitopes for WBSCR16 antibodies
AA 1-230
Reactivity
All reactivities for WBSCR16 antibodies
Human
Host
All hosts for WBSCR16 antibodies
Rabbit
Clonality
All clonalities for WBSCR16 antibodies
Polyclonal
Conjugate
All conjugates for WBSCR16 antibodies
This WBSCR16 antibody is un-conjugated
Application
All applications for WBSCR16 antibodies
Western Blotting (WB)
Purpose
WBSCR16 Rabbit pAb
Sequence
MALVALVAGA RLGRRLSGPG LGRGHWTAAG RSRSRREAAE AEAEVPVVQY VGERAARADR VFVWGFSFSG ALGVPSFVVP SSGPGPRAGA RPRRRIQPVP YRLELDQKIS SAACGYGFTL LSSKTADVTK VWGMGLNKDS QLGFHRSRKD KTRGYEYVLE PSPVSLPLDR PQETRVLQVS CGRAHSLVLT DREGVFSMGN NSYGQCGRKV VENEIYSESH RVHRMQDFDG
Cross-Reactivity
Human, Mouse, Rat
Characteristics
Polyclonal Antibodies
Purification
Affinity purification
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 1-230 of human WBSCR16 (NP_110425.2).
Isotype
IgG
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Discover our top product WBSCR16 Primary Antibody
Alternatives
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Application Details
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Application Notes
WB,1:500 - 1:2000
Restrictions
For Research Use only
Handling
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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.
Target Details for WBSCR16
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Target
WBSCR16
(Williams-Beuren Syndrome Chromosome Region 16 (WBSCR16))
Alternative Name
RCC1L (WBSCR16 Products )
Synonyms
5730496C04Rik antibody, AU019812 antibody, RCC1 like antibody, reculator of chromosome condensation 1 like antibody, RCC1L antibody, Rcc1l antibody
Background
This gene encodes a protein containing regulator of chromosome condensation 1-like repeats. The encoded protein may function as a guanine nucleotide exchange factor. This gene is located in a region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. Alternative splicing results in multiple transcript variants.,RCC1L,WBSCR16,RCC1 like,Epigenetics & Nuclear Signaling,RNA Binding,Cell Biology & Developmental Biology,RCC1L
Molecular Weight
38kDa/48kDa/49kDa
Gene ID
81554
UniProt
Q96I51
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