WBSCR22 antibody (C-Term)

Catalog No. ABIN2789228

The Rabbit Polyclonal anti-WBSCR22 antibody has been validated for WB. It is suitable to detect WBSCR22 in samples from Human, Mouse, Rat, Dog, Cow, Guinea Pig, Horse, Pig and Rabbit.

Quick Overview for WBSCR22 antibody (C-Term) (ABIN2789228)

Target: WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))

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

Host: Rabbit

Clonality: Polyclonal

Conjugate: This WBSCR22 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-WBSCR22 Antibody

Binding Specificity: C-Term

Sequence: GGAFERRGIR GHQTRRFPLR MSRRGMVRKS RAWVLEKKER HRRQGREVRP

Predicted Reactivity: Cow: 77%, Dog: 86%, Guinea Pig: 79%, Horse: 86%, Human: 100%, Mouse: 86%, Pig: 86%, Rabbit: 93%, Rat: 86%

Characteristics: This is a rabbit polyclonal antibody against WBSCR22. 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: 298 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 WBSCR22

Target: WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))

Alternative Name: WBSCR22

Background: This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found.
Alias Symbols: HASJ4442, HUSSY-3, MGC19709, MGC2022, MGC5140, PP3381, WBMT
Protein Interaction Partner: VCP, UBC, PKN1, OAS1, ZMYM3, THOC2, WDR74, REM1, PHLPP1, PPIP5K1, CUL3, SUMO2,
Protein Size: 298

Molecular Weight: 32 kDa

Gene ID: 114049

NCBI Accession: NM_001202560, NP_001189489

UniProt: C9K060