WBSCR16 antibody (N-Term)

Catalog No. ABIN2791205

This Rabbit Polyclonal antibody specifically detects WBSCR16 in WB. It exhibits reactivity toward Human, Mouse, Rat, Cow, Dog, Guinea Pig, Horse, Pig and Rabbit.

Quick Overview for WBSCR16 antibody (N-Term) (ABIN2791205)

Target: WBSCR16 (Williams-Beuren Syndrome Chromosome Region 16 (WBSCR16))

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

Host: Rabbit

Clonality: Polyclonal

Conjugate: This WBSCR16 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-WBSCR16 Antibody

Binding Specificity: N-Term

Sequence: GYGFTLLSSK TADVTKVWGM GLNKDSQLGF HRSRKDKTRG YEYVLEPSPV

Predicted Reactivity: Cow: 100%, Dog: 93%, Guinea Pig: 93%, Horse: 86%, Human: 100%, Mouse: 100%, Pig: 100%, Rabbit: 79%, Rat: 100%

Characteristics: This is a rabbit polyclonal antibody against WBSCR16. It was validated on Western Blot.

Purification: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the N-terminal region of Human WBSCR16

Application Details

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

Comment:

Antigen size: 358 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 WBSCR16

Target: WBSCR16 (Williams-Beuren Syndrome Chromosome Region 16 (WBSCR16))

Alternative Name: WBSCR16

Background: This gene encodes an RCC1-like G-exchanging factor. It is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
Alias Symbols: WBSCR16
Protein Interaction Partner: UBC, NME6, ATXN1, BRCA1, SYNCRIP, HNRNPU, RBBP6, ICT1,
Protein Size: 358

Molecular Weight: 40 kDa

Gene ID: 81554

UniProt: Q8IW88