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For research use only.

Verified Samples Verified Samples in WB: Hela, 3T3, RAW264.7, Rat brain, Rat kidney
Verified Samples in IF: Mouse kidney
Dilution WB 1:1000-3000,  IF 1:100-200
Isotype IgG
Host Mouse
Reactivity Human,  Mouse,  Rat
Applications WB,  IF
Clonality Monoclonal
Immunogen Synthetic Peptide
Abbre Histone H2B
Synonyms (testis specific),  H2B,  H2B histone family,  H2B histone family member U,  H2B histone family member U testis specific,  H2B testis,  H2B1A,  H2BFU,  H2BT,  H2ba,  HIST1H2BA,  Histone 1,  Histone H2B,  Histone H2B testi,  Histone cluster 1 H2ba,  bA317E16.3,  member U,  testis
Swissprot
Calculated MW 14 kDa
Observed MW 14 kDa

Western blotting is a method for detecting a certain protein in a complex sample based on the specific binding of antigen and antibody. Different proteins can be divided into bands based on different mobility rates. The mobility is affected by many factors, which may cause the observed band size to be inconsistent with the expected size. The common factors include:

1. Post-translational modifications: For example, modifications such as glycosylation, phosphorylation, methylation, and acetylation will increase the molecular weight of the protein.

2. Splicing variants: Different expression patterns of various mRNA splicing bodies may produce proteins of different sizes.

3. Post-translational cleavage: Many proteins are first synthesized into precursor proteins and then cleaved to form active forms, such as COL1A1.

4. Relative charge: the composition of amino acids (the proportion of charged amino acids and uncharged amino acids).

5. Formation of multimers: For example, in protein dimer, strong interactions between proteins can cause the bands to be larger. However, the use of reducing conditions can usually avoid the formation of multimers.

If a protein in a sample has different modified forms at the same time, multiple bands may be detected on the membrane.

Cellular Localization Cytosol, Nucleus, nuclear chromosome, telomeric region, nucleoplasm, nucleus, Other locations: nucleosome.
Concentration 1 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer, 0.5% protein protectant and 50% glycerol.
Purification Method Protein A purification
Research Areas Cancer,  Epigenetics and Nuclear Signaling
Clone No. 3C3
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
background Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6p22-p21.3. HIST1H2BB (Histone Cluster 1 H2B Family Member B) is a Protein Coding gene. Among its related pathways are DNA Double-Strand Break Repair and Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3. GO annotations related to this gene include sequence-specific DNA binding and protein heterodimerization activity. An important paralog of this gene is HIST1H2BN.
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Unconjugated

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