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Nhs antibody (AA 600-900)
Nhs
Reactivity: Human
WB
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-Nhs Antibody
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Target
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Nhs
(Nance-Horan Syndrome (Congenital Cataracts and Dental Anomalies) (Nhs))
Binding Specificity
AA 600-900
Reactivity
Human
Host
All hosts for Nhs antibodies
Rabbit
Clonality
All clonalities for Nhs antibodies
Polyclonal
Conjugate
All conjugates for Nhs antibodies
This Nhs antibody is un-conjugated
Application
All applications for Nhs antibodies
Western Blotting (WB)
Purpose
NHS Rabbit pAb
Sequence
MDQKDDHQSS SGNWSGSSST CPSQTSETIP PAASPPLTGS SHCDSELSLN TAPHANEDAS VFVTEQYNDH LDKVRGHRAN SFTSTVADLL DDPNNSNTSD SEWNYLHHHH DASCRQDFSP ERPKADSLGC PSFTSMATYD SFLEKSPSDK ADTSSHFSVD TEGYYTSMHF DCGLKGNKSY VCHYAALGPE NGQGVGASPG LPDCAWQDYL DHKRQGRPSI SFRKPKAKPT PPKRSSSLRK SDGNADISEK KEPKISSGQH LPHSSREMKL PLDFANTPSR MENANLPTKQ EPSWINQSEQ G
Cross-Reactivity
Human
Characteristics
Polyclonal Antibodies
Purification
Affinity purification
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 600-900 of human NHS (NP_938011.1).
Isotype
IgG
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Alternatives
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Application Details
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Application Notes
WB,1:200 - 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 Nhs
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Target
Nhs
(Nance-Horan Syndrome (Congenital Cataracts and Dental Anomalies) (Nhs))
Alternative Name
NHS (Nhs Products )
Synonyms
CTRCT40 antibody, CXN antibody, SCML1 antibody, NHS actin remodeling regulator antibody, NHS antibody
Background
This gene encodes a protein containing four conserved nuclear localization signals. The encoded protein functions in eye, tooth, craniofacial and brain development, and it can regulate actin remodeling and cell morphology. Mutations in this gene have been shown to cause Nance-Horan syndrome, and also X-linked cataract-40. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.,NHS,CTRCT40,CXN,SCML1,Neuroscience,NHS
Molecular Weight
160kDa/176kDa/179kDa
Gene ID
4810
UniProt
Q6T4R5
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