FAM161A antibody (C-Term)

Catalog No. ABIN2788447

This Rabbit Polyclonal antibody specifically detects FAM161A in WB. It exhibits reactivity toward Human, Dog, Mouse, Rabbit, Horse, Pig, Cow and Rat.

Quick Overview for FAM161A antibody (C-Term) (ABIN2788447)

Target: FAM161A (Family with Sequence Similarity 161, Member A (FAM161A))

Reactivity: Human, Dog, Mouse, Rabbit, Horse, Pig, Cow, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM161A antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-FAM161A Antibody

Binding Specificity: C-Term

Sequence: CNPPVPTVSS RGREQAVRKS EKERMREYQR ELEEREEKLK KRPLLFERVA

Predicted Reactivity: Cow: 93%, Dog: 93%, Horse: 93%, Human: 100%, Mouse: 79%, Pig: 93%, Rabbit: 90%, Rat: 100%

Characteristics: This is a rabbit polyclonal antibody against FAM161A. It was validated on Western Blot.

Purification: Affinity Purified

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator.

Comment:

Antigen size: 551 AA

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: Lot specific

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.

Handling Advice: Avoid repeated freeze-thaw cycles.

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 FAM161A

Target: FAM161A (Family with Sequence Similarity 161, Member A (FAM161A))

Alternative Name: FAM161A

Background: This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28.
Alias Symbols: FLJ13305, MGC129982, MGC129983, RP28
Protein Interaction Partner: DHX32, NECAB2, TFIP11, MTUS2, ZBTB43, NINL, ZBTB1, MID2, EHMT2, RUNDC3A, PNMA2, IKZF1, TNIP1, CALCOCO2, TMCC2, KIAA0753, PDE4DIP, STX11, CADPS, PPFIA1, ZBTB14, TRAF1, TRIM37, MDFI, MCM6, KRTAP5-9, PHC2, CDR2, ZBTB8A, KRTAP10-3, KRTAP10-9, KRTAP10-7, CEP57
Protein Size: 551

Molecular Weight: 65 kDa

Gene ID: 84140

NCBI Accession: NM_032180, NP_115556

UniProt: Q3B820