Nhs antibody (AA 600-900)

Catalog No. ABIN7268827

This Rabbit Polyclonal antibody specifically detects Nhs in WB. It exhibits reactivity toward Human.

Quick Overview for Nhs antibody (AA 600-900) (ABIN7268827)

Target: Nhs (Nance-Horan Syndrome (Congenital Cataracts and Dental Anomalies) (Nhs))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Nhs antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-Nhs Antibody

Binding Specificity: AA 600-900

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

Application Details

Application Notes: WB,1:200 - 1:2000

Restrictions: For Research Use only

Handling

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

Target: Nhs (Nance-Horan Syndrome (Congenital Cataracts and Dental Anomalies) (Nhs))

Alternative Name: NHS

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