Actl7b antibody (N-Term)

Catalog No. ABIN5533660

This anti-Actl7b antibody is a Rabbit Polyclonal antibody detecting Actl7b in WB. Suitable for Human.

Quick Overview for Actl7b antibody (N-Term) (ABIN5533660)

Target: Actl7b (Actin-Like 7b (Actl7b))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Actl7b antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-Actl7b Antibody

Binding Specificity: AA 69-97, N-Term

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This ACTL7B antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 69-97 amino acids from the N-terminal region of human ACTL7B.

Isotype: Ig Fraction

Application Details

Application Notes: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.46 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Storage Comment: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Target Details for Actl7b

Target: Actl7b (Actin-Like 7b (Actl7b))

Alternative Name: ACTL7B

Background: The protein encoded by this gene is a member of a family of actin-related proteins (ARPs) which share significant amino acid sequence identity to conventional actins. Both actins and ARPs have an actin fold, which is an ATP-binding cleft, as a common feature. The ARPs are involved in diverse cellular processes, including vesicular transport, spindle orientation, nuclear migration and chromatin remodeling. This gene (ACTL7B), and related gene, ACTL7A, are intronless, and are located approximately 4 kb apart in a head-to-head orientation within the familial dysautonomia candidate region on 9q31. Based on mutational analysis of the ACTL7B gene in patients with this disorder, it was concluded that it is unlikely to be involved in the pathogenesis of dysautonomia. Unlike ACTL7A, the ACTL7B gene is expressed predominantly in the testis, however, its exact function is not known.

Molecular Weight: 45 kDa

Gene ID: 10880

UniProt: Q9Y614